Radiation Monitoring Devices, 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 |
| K983768 | MODIFICATION TO GAMMA GUIDANCE SYSTEM | July 2, 1999 |
| K961321 | GAMMA GUIDANCE SYSTEM | February 10, 1997 |