K260260
- 510(k) number
- K260260
- Device name
- Automatic Digital Blood Pressure Monitor (LD-587, LD-528, LD-562, LD-581, LD-521, LD-527, LD-572 & LD-569)
- Applicant
- Honsun (Nantong) Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2026-04-28
- Date received
- 2026-01-28
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K260260.pdf
Official FDA record: K260260
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.