510(k) K242776 ยท MMX Device, Percutaneous Retrieval
LimFlow V-Ceiver
| Applicant | LimFlow, Inc., Irvine CA, US |
| Decision | Substantially Equivalent, Feb 14, 2025 |
| Received | Sep 13, 2024 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K242776
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.