K242623
- 510(k) number
- K242623
- Device name
- Disposable Blood Pressure cuff; Reusable Blood Pressure cuff
- Applicant
- Shenzhen Medke Technology Co., Ltd. CN
- Product code
- DXQ — Blood Pressure Cuff
- Decision date
- 2024-10-31
- Date received
- 2024-09-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 1.1 MB · U.S. public domain
Also available from FDA: K242623.pdf
Official FDA record: K242623
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.