FDA 510(k) Application Details - K212860

Device Classification Name	Snare, Flexible   More FDA Info for this Device
510(K) Number	K212860
Device Name	Snare, Flexible
Applicant	Steris Corporation 5976 Heisley Road Mentor, OH 44060 US Other 510(k) Applications for this Company
Contact	Carroll Martin Other 510(k) Applications for this Contact
Regulation Number	876.4300   More FDA Info for this Regulation Number
Classification Product Code	FDI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/08/2021
Decision Date	10/07/2021
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