K251751
- 510(k) number
- K251751
- Device name
- Spo2 Sensor CSS032D
- Applicant
- Shenzhen Ykd Technology Co., Ltd. CN
- Product code
- DQA — Oximeter
- Decision date
- 2025-12-19
- Date received
- 2025-06-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K251751.pdf
Official FDA record: K251751
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.