FDA 510(k) Application Details - K023903

Device Classification Name

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510(K) Number K023903
Device Name WILSON-COOK ENDOSCOPIC CLIPPING DEVICE
Applicant WILSON-COOK MEDICAL, INC.
4900 BETHANIA STATION RD.
WINSTON-SALEM, NC 27105 US
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Contact MARGARET POSNER
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Regulation Number

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Classification Product Code PKL
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Date Received 11/22/2002
Decision Date 02/20/2003
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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