510(k) K222683 ยท LLZ System, Image Processing, Radiological
Fibroid Mapping Reviewer Application (FMRA)
| Applicant | Nesa Medtech Private Limited, Bengaluru, IN |
| Decision | Substantially Equivalent, Jul 17, 2023 |
| Received | Sep 6, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K222683
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.