# Cambridge Medical Instruments, Inc.

- Location (FDA's records): Ossining, NY
- FDA decisions: 8 (1985–1990): 8 510(k) clearances
- Product codes: DPS (4), DSI (2), DSH (1), IOL (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K896771: Ekg, Ecg Kenz, Ecg 302 (Feb 26, 1990)
- K896772: Ekg, Ecg Kenz, Ecg 303 (Feb 26, 1990)
- K895961: Model MC6500 Electrocardiograph (Jan 4, 1990)
- K883454: MC6700 Multi-Channel Electrocardiograph (Jan 25, 1989)
- K871993: MC 6000 Multi-Channel Electrocardiograph (Nov 23, 1987)
- K862748: Model SC-1000 Electrocardiograph Specification (Aug 25, 1986)
- K854282: Preview XT (Jan 8, 1986)
- K854283: Cambridge Model XT1000 (Nov 13, 1985)

Source page: https://510kreport.com/company/cambridge-medical-instruments