FDA 510(k) Application Details - K120204

Device Classification Name	Clamp, Vascular, Reprocessed   More FDA Info for this Device
510(K) Number	K120204
Device Name	Clamp, Vascular, Reprocessed
Applicant	STERILMED, INC. 11140 73RD AVE. NORTH MAPLE GROVE, MN 55369 US Other 510(k) Applications for this Company
Contact	JASON SKRAMSTED Other 510(k) Applications for this Contact
Regulation Number	870.4450   More FDA Info for this Regulation Number
Classification Product Code	NMF Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	01/23/2012
Decision Date	04/03/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	CV - Cardiovascular
Review Advisory Committee	CV - Cardiovascular
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review