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Kev Connecticut Diagnostics, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K913456 VISI-NEISSERIAJSX1991-10-11 View
510(k) K910537 VISI-STREPLQL1991-04-12 View
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