Sqi Diagnostics Systems, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K140691 | IG_PLEX CELIAC DGP PANEL | November 6, 2014 |
| K102490 | IGX PLEX CELIAC QUALITATIVE ASSAY | June 2, 2011 |
| K083080 | IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORM | October 29, 2009 |