510(k) K021150 ยท GKH Apparatus, Automated Blood Cell Diluting
COULTER CELLPREP
| Applicant | Beckman Coulter, Inc., Miami FL, US |
| Decision | Substantially Equivalent, Jun 11, 2002 |
| Received | Apr 10, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K021150
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.