510(k) K852178

EXU-BAG CSU-1200(DISPOS)CANISTER 602-2(NON-DISPOS by American Omni Medical, Inc. — Product Code CAC

K852178 is an FDA 510(k) premarket notification submitted by American Omni Medical, Inc. for the device "EXU-BAG CSU-1200(DISPOS)CANISTER 602-2(NON-DISPOS". The FDA issued a decision of Substantially Equivalent on December 27, 1985. The device falls under product code CAC (Apparatus, Autotransfusion), a Class II device regulated under 21 CFR 868.5830. American Omni Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1985
Date Received
May 20, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Apparatus, Autotransfusion
Device Class
Class II
Regulation Number
868.5830
Review Panel
CV
Submission Type