K241351
- 510(k) number
- K241351
- Device name
- Blood Pressure Monitor (TMB-2092-G)
- Applicant
- Guangdong Transtek Medical Electronics Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2024-08-21
- Date received
- 2024-05-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K241351.pdf
Official FDA record: K241351
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.