K233130
- 510(k) number
- K233130
- Device name
- Blood Pressure Monitor
- Applicant
- Guangdong Transtek Medical Electronics Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2023-12-20
- Date received
- 2023-09-27
- 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: K233130.pdf
Official FDA record: K233130
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.