UNISCAN 24 ECG ROCORDER— 510(k) K920572

Substantially Equivalent

Uniscan , Ltd.

FDA 510(k) clearance K920572 for UNISCAN 24 ECG ROCORDER, Substantially Equivalent on 1992-04-06. Applicant: Uniscan , Ltd..

Clearance details

Applicant: Uniscan , Ltd.
Product code: Code DSH
Advisory panel: Cardiovascular
Date received: 1992-02-07
Decision date: 1992-04-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Camarillo, CA, US

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Adverse events under product code DSH

product code DSH

Death: 3
Injury: 652
Total: 655

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.