K234110
- 510(k) number
- K234110
- Device name
- Belun Ring BLR-200 (BLR-200)
- Applicant
- Belun Technology Company Limited HK
- Product code
- DQA — Oximeter
- Decision date
- 2024-10-11
- Date received
- 2023-12-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K234110.pdf
Official FDA record: K234110
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.