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To: Chartgod who wrote (30)3/11/1998 9:41:00 AM
From: InsideFDA  Read Replies (1) of 99
 
FDA Approval for Sonotron is a done deal. FDA is merely going through the motions at this point -- so say my sources inside the FDA.

And i have to say, it makes complete sense given Sonotron's current wide spread approval across the globe. Now that the device has had some time in the mainstream and no safety issues have arisen, the FDA is very comfortable with bringing this device into the US. (Unfortunately, the FDA often prefers a device be tested in foreign nations -- or on foreigners -- before they will even think of letting it be tested on Americans. Sad but true.)

These developments do little to surprise me as I've had faith in the technology for some time. Its a highly cost effective treatment for a wide variety of non-descript blood borne infections.

The device will be readily accepted by medical organizations and HMO's eager to cut costs, as this specific treatment can drastically reduce the chances of a slight misdiagnosis prolonging overall treatment times -- such is the case with antibiotics. Often times patients are allergic or the bacteria itself has become resistant to a given anti-biotic. These scenarios are completely eliminated with UV treatment.

Those two factors combined -- quick acceptance by HMO's and reduced treatment times covering a wide spectrum of possible infections -- could very well make the Sonotron the next block buster medical device product of this decade.
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