510(k) K150754 ยท MXK Device, Analysis, Anterior Segment
ARGOS
| Applicant | Santec Corporation, Komaki, JP |
| Decision | Substantially Equivalent, Oct 2, 2015 |
| Received | Mar 23, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150754
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.