FDA 510(k) Application Details - K964120

Device Classification Name	Forceps, Biopsy, Non-Electric   More FDA Info for this Device
510(K) Number	K964120
Device Name	Forceps, Biopsy, Non-Electric
Applicant	ROBERT J. JYNCH, JR. 124 FISK AVE. PITTSBURGH, PA 15202 US Other 510(k) Applications for this Company
Contact	ROBERT J JYNCH, JR. Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	FCL Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	10/15/1996
Decision Date	12/30/1996
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