FDA 510(k) Application Details - K964979

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K964979
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	POROUS MEDIA CORP. 1350 HAMMOND RD. ST. PAUL, MN 55110 US Other 510(k) Applications for this Company
Contact	KEITH A ROBERTS 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	12/12/1996
Decision Date	03/11/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	HO - General Hospital
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review