K251331
- 510(k) number
- K251331
- Device name
- Blood Pressure Monitor (B73, BE23T)
- Applicant
- Shenzhen Jamr Technology Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-10-27
- Date received
- 2025-04-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K251331.pdf
Official FDA record: K251331
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.