FDA 510(k) Application Details - K032322

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K032322
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	INTERSURGICAL, INC. 417 ELECTRONICS PKWY. LIVERPOOL, NY 13088 US Other 510(k) Applications for this Company
Contact	MICHAEL ZALEWSKI 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	07/28/2003
Decision Date	05/13/2004
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