510(k) K073508 ยท MXK Device, Analysis, Anterior Segment
PARKONE
| Applicant | Oculus Optikgerate GmbH, Wetzlar, DE |
| Decision | Substantially Equivalent, Sep 11, 2008 |
| Received | Dec 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073508
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.