FDA applicant

Cambridge Medical Technology

Billerica, MA14 decisions1982–19890 recalls

FDA records 14 decisions for Cambridge Medical Technology (Billerica, MA) from 1982 to 1989: 14 510(k) clearances. Most are in product codes CDZ (Radioimmunoassay, Testosterones And…) and CGR (Radioimmunoassay, Cortisol). 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 Medical Technology’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cambridge Medical Technology since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cambridge Medical Technology 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 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 Technologies, Inc. 2

Cambridge Medical Technology

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cambridge”