510(k) K261759 ยท LOX Catheters, Transluminal Coronary Angioplasty, Percutaneous
Euphora Rapid Exchange (RX) Balloon Dilatation Catheter
| Applicant | Medtronic Ireland, Galway, IE |
| Decision | Substantially Equivalent, Jul 27, 2026 |
| Received | May 28, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K261759
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.