510(k) K191051 ยท MXK Device, Analysis, Anterior Segment
ARGOS
| Applicant | Santec Corporation, Komaki, JP |
| Decision | Substantially Equivalent, May 16, 2019 |
| Received | Apr 19, 2019 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K191051
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.