510(k) K160561
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 2, 2016
- Date Received
- February 29, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Catheter, Percutaneous
- Device Class
- Class II
- Regulation Number
- 870.1250
- Review Panel
- CV
- Submission Type