510(k) K232443 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, Sep 7, 2023 |
| Received | Aug 14, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K232443
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.