FDA 510(k) Application Details - K030271

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K030271
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	VENTLAB CORP. 2934 HWY. 601 NORTH MOCKSVILLE, NC 27028 US Other 510(k) Applications for this Company
Contact	ROBERT M KELLY 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	01/27/2003
Decision Date	07/07/2003
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