510(k) K013037
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 7, 2001
- Date Received
- September 10, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Fistula
- Device Class
- Class II
- Regulation Number
- 876.5540
- Review Panel
- GU
- Submission Type