510(k) K052717

D732 MICRO 27 PH.I.S.I.O. ADULT ARTERIAL FILTER by Dideco S.R.L. — Product Code DTM

K052717 is an FDA 510(k) premarket notification submitted by Dideco S.R.L. for the device "D732 MICRO 27 PH.I.S.I.O. ADULT ARTERIAL FILTER". The FDA issued a decision of Substantially Equivalent on October 20, 2005. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Dideco S.R.L. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 20, 2005
Date Received
September 29, 2005
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