K260539
- 510(k) number
- K260539
- Device name
- MedSource QuickSafe Safety IV Catheter; MedSource PurSafe Safety IV Catheter
- Applicant
- MedSource Labs, LLC MN · US
- Product code
- FOZ — Catheter, Intravascular, Therapeutic, Short-Term Les
- Decision date
- 2026-07-09
- Date received
- 2026-02-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General Hospital
510(k) Summary (official FDA PDF): K260539.pdf
Official FDA record: K260539
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.