Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP Progress (BP3T01-1B)— 510(k) K251120

Substantially Equivalent

Microlife Corporation

FDA 510(k) clearance K251120 for Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP Progress (BP3T01-1B), Substantially Equivalent on 2025-08-06. Applicant: Microlife Corporation.

Clearance details

Applicant: Microlife Corporation
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2025-04-11
Decision date: 2025-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Taipei, 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.