Technology Marketing Group
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K941715 | ULTATHIN FLEXIBLE ENDOSCOPE | October 4, 1994 |
| K942388 | TAS-(VARIOUS) ULTRATHIN FLEXIBLE ENDOSCOPE | August 17, 1994 |
| K935834 | TAS-211/2.3 ULTRATHIN FLEXIBLE ENDOSCOPE | March 7, 1994 |