510(k) K936003
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 20, 1994
- Date Received
- December 16, 1993
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Reservoir, Blood, Cardiopulmonary Bypass
- Device Class
- Class II
- Regulation Number
- 870.4400
- Review Panel
- CV
- Submission Type