510(k) K162991 ยท IZI System, X-Ray, Angiographic
YELLOW 560 Fluorescence Module
| Applicant | Carl Zeiss Meditec, AG, Jena, DE |
| Decision | Unknown, Jul 24, 2017 |
| Received | Oct 27, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K162991
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.