BLOOD PRESSURE DEVICE, 400 SERIES— 510(k) K781906

Substantially Equivalent

Med-Tek Corp.

FDA 510(k) clearance K781906 for BLOOD PRESSURE DEVICE, 400 SERIES, Substantially Equivalent on 1978-11-16. Applicant: Med-Tek Corp..

Clearance details

Applicant: Med-Tek Corp.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1978-11-13
Decision date: 1978-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

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.