510(k) K090518
K090518 is an FDA 510(k) premarket notification submitted by Maquet Cardiopulmonary, AG for the device "QUART ARTERIAL FILTER WITH SOFTLINE COATING". The FDA issued a decision of Substantially Equivalent on December 18, 2009. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Maquet Cardiopulmonary, AG has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 18, 2009
- Date Received
- February 26, 2009
- 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