FDA 510(k), K902320, BAUER FLEXI-TEMNO BIOPSY NEEDLE

FDA 510(k), K902320, BAUER FLEXI-TEMNO BIOPSY NEEDLE

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510(K) Number: K902320
Device Name: BAUER FLEXI-TEMNO BIOPSY NEEDLE
Manufacturer: PROACT, LTD.
Device Classification Name: biopsy needle
Regulation Number: 876.1075
Classification Product Code: FCG
Date Received: 05/23/1990
Decision Date: 10/01/1990
Regulation Medical Specialty: Gastroenterology/Urology

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