510(k) K242092

MICRO Arterial Filters by Sorin Group Italia S.R.L. — Product Code DTM

K242092 is an FDA 510(k) premarket notification submitted by Sorin Group Italia S.R.L. for the device "MICRO Arterial Filters". The FDA issued a decision of Substantially Equivalent on November 18, 2024. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Sorin Group Italia S.R.L. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 18, 2024
Date Received
July 17, 2024
Clearance Type
Special
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