CARDIOCAP II(TM)— 510(k) K912530

Substantially Equivalent

Datex Medical Instrumentation, Inc.

FDA 510(k) clearance K912530 for CARDIOCAP II(TM), Substantially Equivalent on 1991-09-05. Applicant: Datex Medical Instrumentation, Inc..

Clearance details

Applicant: Datex Medical Instrumentation, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1991-06-07
Decision date: 1991-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tewksbury, MA, US

Download summary PDF View on FDA.gov ↗

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.