BLOOD PRESSURE RECORDER— 510(k) K781932

Substantially Equivalent

Cardiodyne, Inc.

FDA 510(k) clearance K781932 for BLOOD PRESSURE RECORDER, Substantially Equivalent on 1978-11-29. Applicant: Cardiodyne, Inc..

Clearance details

Applicant: Cardiodyne, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1978-11-20
Decision date: 1978-11-29
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.