510(k) K041841 ยท MXK Device, Analysis, Anterior Segment
PACHYCAM
| Applicant | Oculus Optikgerate GmbH, Wetzla-Dutenhofen, DE |
| Decision | Substantially Equivalent, Jan 28, 2005 |
| Received | Jul 8, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K041841
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.