510(k) K841958

CARDIO METRICS CARDIOTOMY RESERVOIR by Sterile Design, Inc. — Product Code JOD

K841958 is an FDA 510(k) premarket notification submitted by Sterile Design, Inc. for the device "CARDIO METRICS CARDIOTOMY RESERVOIR". The FDA issued a decision of Substantially Equivalent on October 15, 1984. The device falls under product code JOD (Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4270. Sterile Design, Inc. has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 15, 1984
Date Received
May 14, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiotomy Suction Line, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4270
Review Panel
CV
Submission Type