K231303
- 510(k) number
- K231303
- Device name
- Arm-type Fully Automatic Digital Blood Pressure Monitor
- Applicant
- Joytech Healthcare Co. , Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2024-01-26
- Date received
- 2023-05-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K231303.pdf
Official FDA record: K231303
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.