K251120
- 510(k) number
- K251120
- Device name
- Microlife Upper Arm Automatic Digital Blood Pressure Monitor, Model BP Progress (BP3T01-1B)
- Applicant
- Microlife Corporation TW
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-08-06
- Date received
- 2025-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.9 MB · U.S. public domain
Also available from FDA: K251120.pdf
Official FDA record: K251120
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.