K253142
- 510(k) number
- K253142
- Device name
- Arm Blood Pressure Monitor (MJ1D,MJ1DS,MJ3D,MJ5D,MJ6D,MJ8D,RN3D,MJ4D,RN1D,RN2D)
- Applicant
- Ningbo Ranor Medical Technology Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2026-01-09
- Date received
- 2025-09-25
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K253142.pdf
Official FDA record: K253142
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.