510(k) K251848 · MXK Device, Analysis, Anterior Segment
Pentacam® Cornea OCT
| Applicant | Oculus Optikgeräte GmbH, Wetzlar, DE |
| Decision | Substantially Equivalent, Mar 13, 2026 |
| Received | Jun 16, 2025 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K251848
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.