K223170
- 510(k) number
- K223170
- Device name
- Electronic Blood Pressure Monitor, model: HTD6602US
- Applicant
- Hetaida Technology Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2023-12-05
- Date received
- 2022-10-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 3.3 MB · U.S. public domain
Also available from FDA: K223170.pdf
Official FDA record: K223170
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.