FDA 510(k) Applications Submitted by SQI DIAGNOSTICS SYSTEMS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K102490 | 08/31/2010 | IGX PLEX CELIAC QUALITATIVE ASSAY | SQI DIAGNOSTICS SYSTEMS |
| K083080 | 10/16/2008 | IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORM | SQI DIAGNOSTICS SYSTEMS |
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