510(k) Report

FDA applicant

Cambridge Medical Instruments, Inc.

Ossining, NY8 decisions1985–19900 recalls

FDA records 8 decisions for Cambridge Medical Instruments, Inc. (Ossining, NY) from 1985 to 1990: 8 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DSI (Detector And Alarm, Arrhythmia). 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, cardiovascular panel, where it files most

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

FDA decisions per year

No FDA decision for Cambridge Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

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Other applicant names beginning “Cambridge”

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