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Cambridge Diagnostics Ireland, Ltd.

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

Total Devices4
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K013907 INVERNESS MEDICAL EARLY PREGNANCY TESTLCX2001-12-18 View
510(k) K970768 HUMAN LYME IGM WESTERN BLOT KITLSR1998-04-09 View
510(k) K970761 LIMITED HUMAN LYME IGG WESTERN BLOT KIT (CAMBRIDGE DIAGNOSTICS IRELAND)LSR1998-04-09 View
510(k) K955903 SELFCARE EARLY PREGNANCY TESTLCX1996-03-06 View
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