FDA 510(k) Application Details - K963717

Device Classification Name	Filter, Conduction, Anesthetic   More FDA Info for this Device
510(K) Number	K963717
Device Name	Filter, Conduction, Anesthetic
Applicant	MILLIPORE CORP. 80 ASHBY RD. P.O. BOX 9125 BEDFORD, MA 01730 US Other 510(k) Applications for this Company
Contact	THOMAS G BORROWS Other 510(k) Applications for this Contact
Regulation Number	868.5130   More FDA Info for this Regulation Number
Classification Product Code	BSN Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	09/16/1996
Decision Date	06/10/1997
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	AN - Anesthesiology
Review Advisory Committee	AN - Anesthesiology
Statement / Summary / Purged Status	Statement
Type	Traditional
Reviewed By Third Party	N
Expedited Review