Nashville Surgical Instruments
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K081366 | KUMAR T-ANCHORS HERNIA SET | July 15, 2008 |
| K973621 | PRE-VIEW CHOLANGIOGRAPHY CLAMP | December 17, 1997 |