K232975
- 510(k) number
- K232975
- Device name
- Pulse Oximeter (MD300C228)
- Applicant
- Beijing Choice Electronic Technology Co., Ltd. CN
- Product code
- DQA — Oximeter
- Decision date
- 2024-06-21
- Date received
- 2023-09-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K232975.pdf
Official FDA record: K232975
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.