VASOTRAC BLOOD PRESSURE MONITOR, MODEL - APM 205— 510(k) K950249

Substantially Equivalent

Medwave, Inc.

FDA 510(k) clearance K950249 for VASOTRAC BLOOD PRESSURE MONITOR, MODEL - APM 205, Substantially Equivalent on 1995-02-01. Applicant: Medwave, Inc..

Clearance details

Applicant: Medwave, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 1995-01-20
Decision date: 1995-02-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, 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.