FDA 510(k), K900770, HOME URODATA SYSTEM(TM)

FDA 510(k), K900770, HOME URODATA SYSTEM(TM)

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510(K) Number: K900770
Device Name: HOME URODATA SYSTEM(TM)
Manufacturer:
Device Classification Name: Uroflowmeter
Regulation Number: 876.1800
Classification Product Code: EXY
Date Received: 02/16/1990
Decision Date: 06/08/1990
Regulation Medical Specialty: Gastroenterology/Urology
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