510(k) K875080

AIR VENT LINE CAT. NO. AVL-36 by American Omni Medical, Inc. — Product Code DTM

K875080 is an FDA 510(k) premarket notification submitted by American Omni Medical, Inc. for the device "AIR VENT LINE CAT. NO. AVL-36". The FDA issued a decision of Substantially Equivalent on February 29, 1988. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. American Omni Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
February 29, 1988
Date Received
December 9, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class
Class II
Regulation Number
870.4260
Review Panel
CV
Submission Type