510(k) K230320 ยท ETN Stimulator, Nerve
NIM Standard Reinforced EMG Endotracheal Tube; CONTACT Reinforced EMG Endotracheal Tube
| Applicant | Medtronic Xomed, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Oct 26, 2023 |
| Received | Feb 6, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K230320
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.