Biomira 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 |
|---|
| K952802 | VISUWELL REAGIN II | May 23, 1996 |
| K932453 | VISUWELL SYPHILIS ANTIBODY | July 11, 1995 |