510(k) K103056 ยท HQF Laser, Ophthalmic
VISULAS TRION LASER SYSTEM WITH THE VITE OPTION
| Applicant | Carl Zeiss Meditec, AG, Dublin CA, US |
| Decision | Substantially Equivalent, Feb 1, 2011 |
| Received | Oct 15, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103056
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.