K261082
- 510(k) number
- K261082
- Device name
- Microlife Wrist Blood Pressure Monitor , (Model BPHJG5-G)
- Applicant
- Microlife Corporation CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2026-07-23
- Date received
- 2026-04-01
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K261082.pdf
Official FDA record: K261082
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.