510(k) K163632 ยท LQJ Lens, Surgical, Laser, Accesssory, Ophthalmic Laser
Katalyst Cyclophotocoagulation Probe
| Applicant | Katalyst Surgical, LLC, Chesterfield MO, US |
| Decision | Substantially Equivalent, Jun 15, 2017 |
| Received | Dec 22, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K163632
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.