FDA 510(k) Application Details - K171916

Device Classification Name	Forceps, Biopsy, Electric   More FDA Info for this Device
510(K) Number	K171916
Device Name	Forceps, Biopsy, Electric
Applicant	Olympus Medical Systems Corp. 2951 Ishikawa-cho Hachioji-shi 192-8507 JP Other 510(k) Applications for this Company
Contact	Toshiyuki Nakajima 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	06/26/2017
Decision Date	10/13/2017
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