510(k) K233391 ยท GWG Endoscope, Neurological
cCeLL - In vivo
| Applicant | VPIX Medical, Inc., Daejeon, KR |
| Decision | Substantially Equivalent, Aug 21, 2024 |
| Received | Oct 2, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K233391
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.