K222511
- 510(k) number
- K222511
- Device name
- Oxy2Pro
- Applicant
- Southmedic, Inc. CA
- Product code
- CCK — Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
- Decision date
- 2023-11-21
- Date received
- 2022-08-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Anesthesiology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K222511.pdf
Official FDA record: K222511
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.