Kev Connecticut Diagnostics, 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 |
|---|
| K913456 | VISI-NEISSERIA | October 11, 1991 |
| K910537 | VISI-STREP | April 12, 1991 |