Diatech Diagnostica , Ltd.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K895276 | DIATECH IGM-MP TEST | December 18, 1989 |
| K882596 | MP TEST | June 21, 1989 |
| K882211 | URISCREEN | September 30, 1988 |