510(k) K222083 ยท MMX Device, Percutaneous Retrieval
LimFlow V-Ceiver
| Applicant | LimFlow, Inc., San Jose CA, US |
| Decision | Substantially Equivalent, Aug 9, 2022 |
| Received | Jul 15, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222083
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.