Kevtek Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K902193 | KEVTEK LASER-STOP ENDOTRACHEAL TUBE LASER-STOP | March 15, 1991 |
| K902000 | KEVTEK(TM) LASER DRAPE/ORGAN PROTECTOR/EYE SHIELD | August 21, 1990 |