510(k) K100684 ยท GKH Apparatus, Automated Blood Cell Diluting
CELLTRACKS AUTOPREP SYSTEM MODEL:9541
| Applicant | Veridex, LLC, Raritan NJ, US |
| Decision | Substantially Equivalent, Aug 26, 2010 |
| Received | Mar 10, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100684
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.