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Sqi Diagnostics Systems

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K102490 IGX PLEX CELIAC QUALITATIVE ASSAYMVM2011-06-02 View
510(k) K083080 IGX PLEX RHEUMATOID ARTHRITIS (RA) ASSAY AND SQIDWORKS DIAGNOSTICS PLATFORMDHR2009-10-29 View
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