FDA applicant

Cambridge Technologies, Inc.

Cambridge, MD2 decisions1987–19880 recalls

FDA records 2 decisions for Cambridge Technologies, Inc. (Cambridge, MD) from 1987 to 1988: 2 510(k) clearances. Most are in product codes FOX (Stand, Infusion) and FPO (Stretcher, Wheeled). 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, general hospital panel, where it files most

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

FDA decisions per year

No FDA decision for Cambridge Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Cambridge Technologies, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

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 Technologies, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Cambridge”