EKG, ECG KENZ, ECG 302— 510(k) K896771

Substantially Equivalent

Cambridge Medical Instruments, Inc.

FDA 510(k) clearance K896771 for EKG, ECG KENZ, ECG 302, Substantially Equivalent on 1990-02-26. Applicant: Cambridge Medical Instruments, Inc..

Clearance details

Applicant: Cambridge Medical Instruments, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 1989-12-01
Decision date: 1990-02-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ossining, NY, US

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Adverse events under product code DSI

product code DSI

Death: 170
Injury: 729
Malfunction: 10,680
Total: 11,579

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.