K242876
- 510(k) number
- K242876
- Device name
- Pulse Oximeter ( PO2, PO2A, PO2B)
- Applicant
- Shenzhen Viatom Technology Co., Ltd. CN
- Product code
- DQA — Oximeter
- Decision date
- 2025-02-28
- Date received
- 2024-09-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Cardiovascular
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242876.pdf
Official FDA record: K242876
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.