Cambridge Diagnostics Ireland, Ltd.

Cambridge Diagnostics Ireland, Ltd. holds 4 FDA 510(k) medical device clearances, first cleared 1996, most recent 2001.

Top product codes for Cambridge Diagnostics Ireland, Ltd.

LCX — Clinical Chemistry2 devices
LSR — Microbiology2 devices

Recent clearances by Cambridge Diagnostics Ireland, Ltd.

K013907 — INVERNESS MEDICAL EARLY PREGNANCY TESTCode LCX·2001-12-18
K970761 — LIMITED HUMAN LYME IGG WESTERN BLOT KIT (CAMBRIDGE DIAGNOSTICS IRELAND)Code LSR·1998-04-09
K970768 — HUMAN LYME IGM WESTERN BLOT KITCode LSR·1998-04-09
K955903 — SELFCARE EARLY PREGNANCY TESTCode LCX·1996-03-06

Data sourced from openFDA. This site is unofficial and independent of the FDA.