FDA 510(k) Application Details - K022879

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K022879
Device Name	Instrument, Biopsy
Applicant	SANARUS MEDICAL, INC. 5880 WEST LAS POSITAS,SUITE 52 PLEASANTON, CA 94588 US Other 510(k) Applications for this Company
Contact	VINCENT CUTARELLI 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	08/30/2002
Decision Date	09/23/2002
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	GU - Gastroenterology & Urology
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review