K251795
- 510(k) number
- K251795
- Device name
- Wrist automatic blood pressure monitor (LD-735, LD-752, LD-753)
- Applicant
- Honsun (Nantong) Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-10-09
- Date received
- 2025-06-12
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K251795.pdf
Official FDA record: K251795
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.