510(k) K850139

COBE COP FILTER CARDIOPULMONARY PREBYPASS FILTER by Rapid Diagnostic Laboratories, Inc. — Product Code KRJ

K850139 is an FDA 510(k) premarket notification submitted by Rapid Diagnostic Laboratories, Inc. for the device "COBE COP FILTER CARDIOPULMONARY PREBYPASS FILTER". The FDA issued a decision of Substantially Equivalent on April 10, 1985. The device falls under product code KRJ (Filter, Prebypass, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4280. Rapid Diagnostic Laboratories, Inc. has at least 5 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 10, 1985
Date Received
January 14, 1985
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Prebypass, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4280
Review Panel
CV
Submission Type