Diesse Diagnostica Senese S.P.A.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 2
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
| K070062 | COPROSET SALMONELLA AND SHIGELLA, URISET PRESERVATIVE TUBES AND SWAB SET GENERAL USE | July 30, 2007 |
| K050590 | ENZY-WELL SYPHILIS IGG, MODEL 91106 | August 10, 2006 |