FDA applicant

Cambridge Diagnostic Products, Inc.

Ft. Lauderdale, FL1 decision1995–19950 recalls

FDA records 1 decision for Cambridge Diagnostic Products, Inc. (Ft. Lauderdale, FL) in 1995: 1 510(k) clearance. All are in product code LXG (Equipment, Laboratory, General Purpose…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Cambridge Diagnostic Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cambridge Diagnostic Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cambridge Diagnostic Products, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Cambridge”

FDA records each applicant name separately; these may or may not be the same firm.

Cambridge Heart, Inc. 17 Cambridge Medical Technology 14 Cambridge Instruments, Inc. 13 Cambridge Medical Instruments, Inc. 8 Cambridge Bioscience Corp. 5 Cambridge Nuclear Corp. 5 Cambridge Chemical Products, Inc. 4 Cambridge Diagnostics Ireland, Ltd. 4 Cambridge Life Sciences Plc. 4 Cambridge Sensors Limited 3 Cambridge Biotech Corp. 3 Cambridge Scientific 2

Cambridge Diagnostic Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cambridge”