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Allelix Diagnostics, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K885298 VISUWELL REAGIN TEST 960 TEST KITGMP1989-03-15 View
510(k) K880665 MODIFIED GROUP A STREPTOCOCCUS DETECTION KITGTZ1988-03-01 View
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