FDA 510(k) Application Details - K121382

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K121382
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	Westmed, Inc. 5580 S. NOGALES HIGHWAY TUCSON, AZ 85706 US Other 510(k) Applications for this Company
Contact	R. JOHN MCKINNON Other 510(k) Applications for this Contact
Regulation Number	868.5260   More FDA Info for this Regulation Number
Classification Product Code	CAH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	05/08/2012
Decision Date	12/06/2012
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review