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To: blokker who wrote (21545)5/27/1998 9:29:00 AM
From: Don Powrie  Respond to of 34592
 
>>>>NEWS! Nasdaq: ECIN

EMCEE Announces Wireless High Speed Internet Service

WHITE HAVEN, Pa., May 27 /PRNewswire/ -- EMCEE Broadcast Products, Inc. (Nasdaq: ECIN - news) today announced that it will launch a high speed Internet service in Logan, Utah, using the wireless communications spectrum known as MMDS. Subscribers can receive Internet service at speeds more than 100 times faster than a traditional wired Internet service.

EMCEE and the Basic Trading Area (BTA) holder, Phil Merrill, have formed Universal Rapid Access (URA) to provide wireless communications services in the Logan, Utah, area. The initial service will use the wireless MMDS spectrum for downstream communication and telephone return path for upstream communication. URA has filed an application with the Federal Communications Commission for a two-way RF license. If granted, URA will offer two-way RF service to those subscribers requiring the greater upstream and downstream capacity afforded by a two-way RF system.

John Saul, Vice President -- Systems Engineering for EMCEE, stated, ''This new downstream wireless approach is considerably more economical in terms of capital costs since it
is essentially free of the requirement for physical wired infrastructure. More importantly, this new method of Internet service enables downstream speeds of up to 10 Megabits per
second within each of the three 2 Megahertz subchannels for an aggregate of nearly 30 Megabits per second in a 6 Megahertz channel. These greater speeds are possible because
of the broadband nature of the microwave channel as opposed to conventional copper telephone lines which currently limit speeds to less than 33.6 Kilobits per second. While the
system will initially be built with a telephone line return, planning is already underway for upgrading the system for wireless return. This architecture will permit upstream speeds of up
to 2 Megabits per second which will further enhance the attractiveness of the system.''

Saul continued, ''EMCEE is making this investment to better understand the overall operation of high speed Internet systems using the wireless MMDS spectrum. The management
of EMCEE believes high speed Internet service in the 2.5 to 2.7 GHZ band is an expanding market and having this experience with URA will position the Company to serve a
broader customer base. EMCEE will continue to seek additional opportunities for high speed Internet service in other markets.''

Phil Merrill commented, ''I am very pleased to be working with a company of EMCEE's stature on the Logan high speed Internet project. This project is the result of collective
efforts between myself and representatives of EMCEE and I look forward to the successful development and launch of the Logan high speed Internet service.''

EMCEE is a global leader in manufacturing and marketing of analog and digital wireless transmitters and associated hardware for the wireless communications (MMDS) industry.
MMDS offers subscribers a mix of broadcast and satellite cable channels by using EMCEE manufactured transmitters to deliver multichannel television plus high speed Internet and
other data applications. Additionally, the Company is a supplier of UHF and VHF low power television transmitters and transmitters for the high definition television (HDTV)
market. EMCEE's products are installed in more than ninety-five (95) countries. For more information visit their web site at www.emceebrd.com.

Universal Rapid Access, a Utah company, is a high speed Internet service provider. Formed in 1998, Universal Rapid Access is owned by a wholly owned subsidiary of EMCEE
and the frequency license holder, Phil Merrill, a long time industry entrepreneur.

Certain statements in this release contain forward-looking statements that involve risks and uncertainties, including without limitation, product demand, competitive products and
pricing, market acceptance of products and services including but not limited to high-speed Internet service, video and telephony applications, technological changes, current and
future domestic and international economic conditions and other risks and uncertainties that are detailed from time to time in the Company's SEC reports. Copies of the Company's
most recent Form 10-QSB and Form 10-KSB can be obtained from the Company on request.

SOURCE: EMCEE Broadcast Products, Inc.



To: blokker who wrote (21545)5/27/1998 9:30:00 AM
From: Don Powrie  Respond to of 34592
 
>>>>NEWS! Nasdaq: NMPS

Matritech Announces Approval in Japan of the NMP22(R) Test Kit for Both Monitoring and Screening of Bladder Cancer Patients

Test to be Marketed and Distributed by Konica Corporation

NEWTON, Mass., May 27 /PRNewswire/ -- Matritech, Inc., (Nasdaq: NMPS - news) announced today that they have been informed by their Japanese marketing partner for NMP22, Konica Corporation, that the Japanese Ministry of Health and Welfare has approved Matritech's NMP22(R) Test Kit for monitoring as well as the testing of high risk,
previously undiagnosed bladder cancer patients. The test will be distributed in Japan by Konica Corporation, an international leader in the manufacturing, marketing and sales of photographic products, business machines, medical products and graphic arts products. NMP22 is the first quantitative screening test for individuals who are at high risk for bladder cancer to receive approval in Japan.

The NMP22(R) Test Kit is based on Matritech's proprietary nuclear matrix protein (NMP) technology, which correlates levels of NMPs in body fluids to the presence of cancer. The product is currently approved in the United States and Europe for the management of patients with transitional cell carcinoma of the urinary tract.

''The Japanese Ministry's approval of the NMP22 test for both patient management and screening is a significant endorsement of the broad utility of both NMP22 and our proprietary nuclear matrix protein technology,'' commented David L. Corbet, President and Chief Operating Officer of Matritech, Inc. ''Multiple clinical studies published in Japan, Europe and the United States have demonstrated NMP22's ability to detect previously undiagnosed bladder cancer. Matritech plans to pursue approval of similar claims with the Food and Drug Administration in the United States.''

''The urology community in Japan has demonstrated a strong commitment to using quality diagnostic methods,'' said Mr. Shigeru Suzuki, Director, Senior General Manager,
Medical Imaging Division, Konica Corporation. ''Based on NMP22's accuracy and simplicity, we are optimistic that the adoption of this product will make a significant contribution
to improving the care of bladder cancer patients in Japan.''

Konica Corporation, based in Tokyo, Japan, is a leading Japanese company in the global photographic and information imaging industries that is recognized for the excellence and
innovativeness of its products. The company, established in 1873, celebrates the 125th anniversary this year. In the field of medical products, the company was the first manufacturer
of X-ray films in Japan. Since then, Konica has continued to develop various medical diagnostic imaging systems. Today, with the addition of digital imaging technology and
biotechnology, its extensive medical product lineup, from X-ray film and processors to digital imaging systems, laser imagers and diagnostic reagent are well-known for superb
quality and performance.

Matritech, Inc., based in Newton, Massachusetts, is using its proprietary nuclear matrix protein (NMP) technology, discovered at the Massachusetts Institute of Technology (MIT)
and licensed exclusively to Matritech, to develop and commercialize innovative serum-, cell-, and urine-based NMP diagnostics that enable physicians to reliably detect and monitor
the presence of bladder, colon, cervical, breast and prostate cancers.

Any forward looking statements related to the Company's expectations regarding the performance, benefits to patients, market acceptance, future sales and regulatory approvals of
the Company's existing and future products are subject to a number of risks and uncertainties, many of which are beyond the Company's control. These include but are not limited
to, risks related to incorrect use of products by customers, unforeseen delays in or denials of FDA and other regulatory approvals, future product demand and pricing, performance
of distributors, competitive products and technical developments, health care reform and general business and economic conditions. There can be no assurance that the Company's
expectations for its product will be achieved.