FDA applicant
Cambridge Medical Instruments, Inc.
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
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.
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.
See the 510(k) ReportOther applicant names beginning “Cambridge”
FDA records each applicant name separately; these may or may not be the same firm.