Marlow Surgical Technologies, 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 |
| K964848 | WALLACE ARTIFICIAL INSEMINATION CATHETER - 8CM/18CM | January 16, 1997 |
| K944563 | FAMILY OF PRIMUS FORCEPS: GRASPERS/DISSECTORS/SUTURERS/NEEDLE DRIVERS | December 27, 1994 |