FDA 510(k) Application Details - K131157

Device Classification Name	Instrument, Biopsy   More FDA Info for this Device
510(K) Number	K131157
Device Name	Instrument, Biopsy
Applicant	RANFAC CORP. 30 Doherty Avenue, P.O. Box 635 Avon Industrial Park Avon, MA 02322 US Other 510(k) Applications for this Company
Contact	CHRISTOPHER P WHELAN 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	04/24/2013
Decision Date	10/22/2013
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