K241431
- 510(k) number
- K241431
- Device name
- Arm-type Fully Automatic Digital Blood Pressure Monitor (DBP-62D0L, DBP-62D0B, DBP-61D0, DBP-61D0L, DBP-6293L, DBP-6293B, DBP-6193)
- Applicant
- Joytech Healthcare Co. , Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-01-13
- Date received
- 2024-05-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.9 MB · U.S. public domain
Also available from FDA: K241431.pdf
Official FDA record: K241431
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.