FDA 510(k) Application Details - K971204

Device Classification Name	Forceps, Biopsy, Electric   More FDA Info for this Device
510(K) Number	K971204
Device Name	Forceps, Biopsy, Electric
Applicant	LSVP INTL., INC. 12755 ALTO VERDE LN. LOS ALTOS HILLS, CA 94022 US Other 510(k) Applications for this Company
Contact	SOPHIA PESOTCHINSKY Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	KGE Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	04/01/1997
Decision Date	05/27/1997
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