FDA 510(k) Application Details - K973215

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K973215
Device Name	Instrument, Biopsy
Applicant	LAURUS MEDICAL CORP. 10 CHRYSLER, SUITE B IRVINE, CA 92618 US Other 510(k) Applications for this Company
Contact	RICHARD A BASLER Other 510(k) Applications for this Contact
Regulation Number	876.1075   More FDA Info for this Regulation Number
Classification Product Code	KNW Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	08/27/1997
Decision Date	11/06/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review