510(k) K884640

CARDIOPLEGIA OVERPRESSURE VALVE CPOP-350 & 700 by American Omni Medical, Inc. — Product Code KRI

K884640 is an FDA 510(k) premarket notification submitted by American Omni Medical, Inc. for the device "CARDIOPLEGIA OVERPRESSURE VALVE CPOP-350 & 700". The FDA issued a decision of Substantially Equivalent on January 24, 1989. The device falls under product code KRI (Accessory Equipment, Cardiopulmonary Bypass), a Class I device regulated under 21 CFR 870.4200. American Omni Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 24, 1989
Date Received
November 7, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Accessory Equipment, Cardiopulmonary Bypass
Device Class
Class I
Regulation Number
870.4200
Review Panel
CV
Submission Type