510(k) K093521 ยท MYC Ophthalmoscope, Laser, Scanning
GDXPRO
| Applicant | Carl Zeiss Meditec, Inc., Dublin CA, US |
| Decision | Substantially Equivalent, Nov 25, 2009 |
| Received | Nov 13, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K093521
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.