510(k) K022331 ยท GKL Counter, Cell, Automated (Particle Counter)
ADVIA 120 HEMATOLOGY SYSTEM, CEREBROSPINAL FLUID METHOD
| Applicant | Bayer Diagnostics Corp., Tarrytown NY, US |
| Decision | Substantially Equivalent, Sep 11, 2002 |
| Received | Jul 18, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022331
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.