510(k) K260539 · FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
MedSource QuickSafe Safety IV Catheter; MedSource PurSafe Safety IV Catheter
| Applicant | MedSource Labs, LLC, Chanhassen MN, US |
| Decision | Substantially Equivalent, Jul 9, 2026 |
| Received | Feb 17, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260539
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.