Murex 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 |
| K962028 | WELLCOLEX E-COLI OI57 ZC60 | November 1, 1996 |
| K954920 | MUREX RUB-EX | August 21, 1996 |