FDA 510(k) Application Details - K024011

Device Classification Name	Forceps, Biopsy, Electric, Reprocessed   More FDA Info for this Device
510(K) Number	K024011
Device Name	Forceps, Biopsy, Electric, Reprocessed
Applicant	SURGICAL INSTRUMENTS SERVICE AND SAVINGS, INC. 723 CURTIS CT; PO BOX 2060 SISTERS, OR 97759 US Other 510(k) Applications for this Company
Contact	MARY ANN BARKER Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	NLU Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	12/04/2002
Decision Date	12/19/2002
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	Y
Expedited Review