510(k) K080595 ยท JOY Device, Automated Cell-Locating
CELLAVISION DM96 WITH THE BODY FLUID APPLICATION
| Applicant | CellaVision AB, Minneapolis, MN, US |
| Decision | Substantially Equivalent, Dec 5, 2008 |
| Received | Mar 3, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080595
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.