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Adi Diagnostics, Inc.

FDA 510(k) & PMA Approved Devices — 4 products

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K910487 VISUWELL SYPHILIS ANTIGENLIP1991-06-24 View
510(k) K900973 VISUWELL(R) CHLAMYDIALJC1990-05-15 View
510(k) K900338 VISUWELL(R) REAGIN TEST (MODIFICATION)GMQ1990-04-10 View
510(k) K890840 VISUWELL GROUP A STREPTOCOCCUS DETECTION KITGTZ1989-03-27 View
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