510(k) K232202 ยท PSY Whole Slide Imaging System
Aperio GT 450 DX
| Applicant | Leica Biosystems Imaging, Inc., Vista CA, US |
| Decision | Substantially Equivalent, Apr 16, 2024 |
| Received | Jul 25, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K232202
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.