510(k) K182431 ยท LLZ System, Image Processing, Radiological
Konicaminolta DI-X1
| Applicant | Konica Minolta, Inc., Hino-Shi, JP |
| Decision | Substantially Equivalent, Nov 26, 2018 |
| Received | Sep 6, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182431
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.