510(k) K173371 ยท HNO Keratome, Ac-Powered
VisuMax Femtosecond Laser
| Applicant | Carl Zeiss Meditec, Inc., Dublin CA, US |
| Decision | Substantially Equivalent, Apr 13, 2018 |
| Received | Oct 27, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K173371
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.