510(k) K833477

INTERSEPT 40 MICRON FILTER by Extracorporeal Medical Specialities, Inc. — Product Code DTM

K833477 is an FDA 510(k) premarket notification submitted by Extracorporeal Medical Specialities, Inc. for the device "INTERSEPT 40 MICRON FILTER". The FDA issued a decision of Substantially Equivalent on December 27, 1983. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Extracorporeal Medical Specialities, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 27, 1983
Date Received
October 7, 1983
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