Sur-Med Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K903401 | SPECIAL RONGEUR | August 10, 1990 |
| K870897 | KODNER ANAL PERIONEAL RETRACTOR | June 4, 1987 |
| K870978 | T-TUBE INSERTER | March 19, 1987 |