510(k) K071183 ยท MXK Device, Analysis, Anterior Segment
ALLEGRO OCULYZER
| Applicant | Wavelight AG, Erlangen, DE |
| Decision | Substantially Equivalent, Jul 20, 2007 |
| Received | Apr 30, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071183
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.