Blairden Precision Instruments, 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 |
|---|
| K932115 | ROWDEN UTERINE MANIPULATOR INJECTOR AND RUMI | June 24, 1994 |
| K912761 | SURGICAL SAW BLADES | July 19, 1991 |