Tenet Medical Engineering
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K963505 | TENET MLTI-POSITIONING SURGICAL STIRRUP SYSTEM | February 14, 1997 |
| K963506 | TENET RADIOLUCENT HAND TABLE | January 9, 1997 |
| K964102 | TENET TIBIAL FRACTURE SUPPORT | December 5, 1996 |