510(k) K923530 ยท GKH Apparatus, Automated Blood Cell Diluting
COULTER MULTI-Q-PREP
| Applicant | Coulter Electronics, Inc., Hialeah FL, US |
| Decision | Substantially Equivalent, Oct 14, 1992 |
| Received | Jul 16, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K923530
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.