510(k) K882137

EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40 by Medtronic Blood Systems, Inc. — Product Code DTM

K882137 is an FDA 510(k) premarket notification submitted by Medtronic Blood Systems, Inc. for the device "EXTENDED SHELF LIFE FOR INTERSEPT* ARTERIAL 20/40". The FDA issued a decision of Substantially Equivalent on August 12, 1988. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Medtronic Blood Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 12, 1988
Date Received
May 20, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class
Class II
Regulation Number
870.4260
Review Panel
CV
Submission Type