Accurate 24 Non-invasive blood pressure monitor— 510(k) K222658

Substantially Equivalent

Accurate Meditech, Inc.

FDA 510(k) clearance K222658 for Accurate 24 Non-invasive blood pressure monitor, Substantially Equivalent on 2023-06-21. Applicant: Accurate Meditech, Inc..

Clearance details

Applicant: Accurate Meditech, Inc.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2022-09-02
Decision date: 2023-06-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: New Taipei City, TW

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.