CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512— 510(k) K900246

Substantially Equivalent

Ppg Industries, Inc.

FDA 510(k) clearance K900246 for CARDIOTEST EK 53 R, CARDIOGNOST EK 56/ EK 512, Substantially Equivalent on 1990-07-03. Applicant: Ppg Industries, Inc..

Clearance details

Applicant: Ppg Industries, Inc.
Product code: Code DSI
Advisory panel: Cardiovascular
Date received: 1990-01-17
Decision date: 1990-07-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pleasantville, 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.