510(k) K260304 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal
WAVE PTA Balloon Catheter
| Applicant | WAVE Medical AG, Neuhausen Am Rheinfall, CH |
| Decision | Substantially Equivalent, May 20, 2026 |
| Received | Jan 30, 2026 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K260304
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.