Geneohm Sciences Canada, 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 |
|---|
| K133605 | BD MAX MRSA XT, BD MAX INSTRUMENT | December 20, 2013 |
| K061686 | IDI-VANR ASSAY | August 30, 2006 |