Gamma Medical Products, 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 |
| K833275 | GMP CIQ ELISA TEST KIT | June 22, 1984 |
| K823009 | GAMMA CLQ | November 5, 1982 |