510(k) K885332 ยท GKL Counter, Cell, Automated (Particle Counter)
COULTER FLOW RETICULOCYTE REAGENT
| Applicant | Coulter Electronics, Inc., Hialeah FL, US |
| Decision | Substantially Equivalent, Feb 22, 1989 |
| Received | Dec 28, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885332
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.