510(k) K960974

COBE CENTURY PERFUSION PUMP by Cobe Cardiovascular, Inc. — Product Code DWB

K960974 is an FDA 510(k) premarket notification submitted by Cobe Cardiovascular, Inc. for the device "COBE CENTURY PERFUSION PUMP". The FDA issued a decision of Substantially Equivalent on July 14, 1997. The device falls under product code DWB (Pump, Blood, Cardiopulmonary Bypass, Roller Type), a Class II device regulated under 21 CFR 870.4370. Cobe Cardiovascular, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 14, 1997
Date Received
March 11, 1996
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pump, Blood, Cardiopulmonary Bypass, Roller Type
Device Class
Class II
Regulation Number
870.4370
Review Panel
CV
Submission Type