510(k) K935953 ยท GKH Apparatus, Automated Blood Cell Diluting
COULTER MULTI Q PREP
| Applicant | Coulter Corp., Miami FL, US |
| Decision | Substantially Equivalent, Mar 11, 1994 |
| Received | Dec 13, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K935953
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.