510(k) K193507 ยท MMX Device, Percutaneous Retrieval
Merit ONE Snare System
| Applicant | Merit Medical Systems, Inc., Galway, IE |
| Decision | Substantially Equivalent, Jan 17, 2020 |
| Received | Dec 18, 2019 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K193507
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.