510(k) K170239 ยท IZI System, X-Ray, Angiographic
Leica FL560
| Applicant | Leica Microsystems (Schweiz) AG, Heerbrugg, CH |
| Decision | Unknown, Jul 5, 2017 |
| Received | Jan 26, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K170239
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.