RECORDER, HOLTER ELECTROCARDIOGRAM— 510(k) K781843

Substantially Equivalent

Hovik Corp.

FDA 510(k) clearance K781843 for RECORDER, HOLTER ELECTROCARDIOGRAM, Substantially Equivalent on 1978-11-03. Applicant: Hovik Corp..

Clearance details

Applicant: Hovik Corp.
Product code: Code DSH
Advisory panel: Cardiovascular
Date received: 1978-11-01
Decision date: 1978-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, 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.