510(k) K983866
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 6, 2000
- Date Received
- November 2, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- System, Balloon, Intra-Aortic And Control
- Device Class
- Class II
- Regulation Number
- 870.3535
- Review Panel
- CV
- Submission Type