510(k) K060053
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 2, 2006
- Date Received
- January 6, 2006
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Console, Heart-Lung Machine, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4220
- Review Panel
- CV
- Submission Type