Siemens Helathcare 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 |
| K131275 | MICROSCAN DRIED GRAM-POSTIVE MIC/COMBO PANELS | November 8, 2013 |
| K132391 | IMMULITE 2000 ANTI-TG AB CALIBRATION VERIFICATION MATERIAL, IMMULITE 2000 ANTI-TPO AB CALIBRATION VE | September 20, 2013 |