K231984
- 510(k) number
- K231984
- Device name
- Clinical Automatic Blood Pressure Monitor (DBP-01P,DBP-01HP)
- Applicant
- Shenzhen Hingmed Medical Instrument Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2024-03-26
- Date received
- 2023-07-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.1 MB · U.S. public domain
Also available from FDA: K231984.pdf
Official FDA record: K231984
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.