510(k) K200268 · MMX Device, Percutaneous Retrieval
Halo Single-Loop Snare Kit
| Applicant | Argon Medical Devices, Inc., Athens TX, US |
| Decision | Substantially Equivalent, Jun 3, 2020 |
| Received | Feb 3, 2020 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K200268
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.