510(k) K061871 ยท IZI System, X-Ray, Angiographic
LEICA MODEL FL800
| Applicant | Leica Microsystems, Inc., Park City UT, US |
| Decision | Substantially Equivalent, Sep 20, 2006 |
| Received | Jul 3, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061871
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.