510(k) K240281 ยท LLZ System, Image Processing, Radiological
Bone Suppression Software
| Applicant | Konica Minolta, Inc., Tokyo, JP |
| Decision | Substantially Equivalent, May 31, 2024 |
| Received | Feb 1, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K240281
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.