510(k) K042251 ยท GKZ Counter, Differential Cell
BAYER ADVIA 2120 HEMATOLOGY ANALYZER WITH AUTOSLIDE SYSTEM
| Applicant | Bayer Healthcare, LLC, Tarrytown NY, US |
| Decision | Substantially Equivalent, Sep 17, 2004 |
| Received | Aug 20, 2004 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K042251
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.