510(k) K002493
K002493 is an FDA 510(k) premarket notification submitted by Cobe Cardiovascular, Inc. for the device "DIDECO MICRO 40 PH.I.S.I.O (PHOSPHORYLCHOLINE INSERT SURFACE IN OXGENATION) NEWBORN/INFANT ARTERIAL FILTER". The FDA issued a decision of Substantially Equivalent on November 30, 2000. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Cobe Cardiovascular, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 30, 2000
- Date Received
- August 14, 2000
- 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