K242721
- 510(k) number
- K242721
- Device name
- Upper Arm Electronic Blood Pressure Monitor (FC-BP103, FC-BP106, FC-BP113, FC-BP120, FC-BP121, FC-BP130, FC-BP131)
- Applicant
- Shenzhen Finicare Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2024-10-04
- Date received
- 2024-09-10
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.2 MB · U.S. public domain
Also available from FDA: K242721.pdf
Official FDA record: K242721
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.