FDA 510(k) Application Details - K142525

Device Classification Name	Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)   More FDA Info for this Device
510(K) Number	K142525
Device Name	Coagulator-Cutter, Endoscopic, Bipolar (And Accessories)
Applicant	Olympus Winter & Ibe GmbH Kuehnstrasse 61 Hamburg 22045 DE Other 510(k) Applications for this Company
Contact	Graham A.L. Baillie Other 510(k) Applications for this Contact
Regulation Number	884.4150   More FDA Info for this Regulation Number
Classification Product Code	HIN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/08/2014
Decision Date	11/21/2014
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	OB - Obstetrics/Gynecology
Review Advisory Committee	OB - Obstetrics/Gynecology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review