510(k) K182659 ยท MXK Device, Analysis, Anterior Segment
Galilei G6 Lens Professional
| Applicant | Sis Ag, Surgical Instrument Systems, Port, CH |
| Decision | Substantially Equivalent, Jul 25, 2019 |
| Received | Sep 25, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K182659
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.