K242255
- 510(k) number
- K242255
- Device name
- Qitexio® 4-Way Stopcock (QIT014)
- Applicant
- Medex FR
- Product code
- FMG — Stopcock, I.V. Set
- Decision date
- 2025-04-29
- Date received
- 2024-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K242255.pdf
Official FDA record: K242255
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.