FDA 510(k) Application Details - K961838

Device Classification Name	Filter, Bacterial, Breathing-Circuit   More FDA Info for this Device
510(K) Number	K961838
Device Name	Filter, Bacterial, Breathing-Circuit
Applicant	MARQUEST MEDICAL PRODUCTS, INC. 11039 EAST LANSING CIR. ENGLEWOOD, CO 80112 US Other 510(k) Applications for this Company
Contact	TOM DIELMANN 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	05/13/1996
Decision Date	10/18/1996
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