510(k) K241587 ยท LJS Catheter, Intravascular, Therapeutic, Long-Term Greater Than 30 Days
pilot TLS
| Applicant | Vygon Corporation, Lansdale Montgomery PA, US |
| Decision | Substantially Equivalent, Feb 26, 2025 |
| Received | Jun 3, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K241587
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.