510(k) K802208 ยท GKL Counter, Cell, Automated (Particle Counter)
LEUKOCYTE VOL. ANALYSIS APPARATUS
| Applicant | Coulter Electronics, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Sep 17, 1980 |
| Received | Sep 11, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802208
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.