510(k) K191758 ยท MMX Device, Percutaneous Retrieval
Single-Loop Snare Retrieval Kit, Triple-Loop Snare Retrieval Kit
| Applicant | Argon Medical Devices, Inc., Athens TX, US |
| Decision | Substantially Equivalent, Dec 17, 2019 |
| Received | Jul 1, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191758
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.