FDA 510(k) Application Details - K961897

Device Classification Name Kit, Needle, Biopsy

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510(K) Number K961897
Device Name Kit, Needle, Biopsy
Applicant WILSON-COOK MEDICAL, INC.
4900 BETHANIA STATION RD.
WINSTON-SALEM, NC 27105 US
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Contact PAULA JOYCE
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Regulation Number 876.1075

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Classification Product Code FCG
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Date Received 05/16/1996
Decision Date 01/29/1997
Decision SESE - SUBST EQUIV
Classification Advisory Committee GU - Gastroenterology & Urology
Review Advisory Committee GU - Gastroenterology & Urology
Statement / Summary / Purged Status Summary
Type Traditional
Reviewed By Third Party N
Expedited Review



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