FDA 510(k) Application Details - K221522

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K221522
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	Olympus Winter & Ibe Gmbh Kuehnstr. 61 Hamburg 22045 DE Other 510(k) Applications for this Company
Contact	Lilly Omland Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/26/2022
Decision Date	01/19/2023
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	GU - Gastroenterology & Urology
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review