K230587
- 510(k) number
- K230587
- Device name
- Wrist Pulse Oximeter
- Applicant
- Beijing Choice Electronic Technology Co., Ltd. CN
- Product code
- DQA — Oximeter
- Decision date
- 2023-11-30
- Date received
- 2023-03-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K230587.pdf
Official FDA record: K230587
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.