Instrumentation Camera, 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 |
|---|
| K810716 | X-RAY IMAGE INTENSIFIER PRODUCTS | April 23, 1981 |
| K802132 | 105MM SPOT FILM CAMERA | October 23, 1980 |