K251102
- 510(k) number
- K251102
- Device name
- Automatic Blood Pressure Monitor (CH-S691L, CH-B607, CH-B606, CH-S692L, CH-S602, CH-W701L, CH-S693L, CH-B601L, CP-B01, CH-S603)
- Applicant
- Cemho Medical Technology (Guangdong) Co., Ltd. CN
- Product code
- DXN — System, Measurement, Blood-Pressure, Non-Invasive
- Decision date
- 2025-07-16
- Date received
- 2025-04-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.3 MB · U.S. public domain
Also available from FDA: K251102.pdf
Official FDA record: K251102
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.