510(k) K261418 ยท EZD Catheter, Straight
Liquick X-treme, Liquick X-treme Plus
| Applicant | Teleflex Medical, Athlone, IE |
| Decision | Substantially Equivalent, Sep 23, 2026 |
| Received | Apr 30, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261418
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.