K240808
- 510(k) number
- K240808
- Device name
- Pulse Oximeter (WS20A)
- Applicant
- Hunan Accurate Bio-Medical Technology Co., Ltd. CN
- Product code
- DQA — Oximeter
- Decision date
- 2024-10-03
- Date received
- 2024-03-25
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240808.pdf
Official FDA record: K240808
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.