510(k) K260080 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
Pro-Line XL Power Injectable Central Venous Catheter and Pro-Line XL Tunneler
| Applicant | Medical Components, Inc., Harleysville PA, US |
| Decision | Substantially Equivalent, Oct 9, 2026 |
| Received | Jan 12, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260080
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.