510(k) K880671

MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER by Medtronic Blood Systems, Inc. — Product Code DTM

K880671 is an FDA 510(k) premarket notification submitted by Medtronic Blood Systems, Inc. for the device "MODIFIED INTERSEPT PEDIATRIC BLOOD FILTER". The FDA issued a decision of Substantially Equivalent on May 6, 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
May 6, 1988
Date Received
February 18, 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