Precision Instruments, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K864520 | BARRON ROTARY BLADE TREPHINE USING HESSBURG-BARRON | January 20, 1987 |
| K860648 | BARRON TWIN BLADE TREPHINE FOR EPPIKARATOPHAKIA | March 25, 1986 |
| K843048 | RING SUPPORTED TREPHINE FOR CORNEA TRANS | October 5, 1984 |
| K801585 | HESSBURG-BFRRON TREPHINE | October 3, 1980 |