510(k) K022512 ยท GKH Apparatus, Automated Blood Cell Diluting
CELLPREP SAMPLE PREPARATION SYSTEM, MODEL 9518
| Applicant | Immunicon Corp., Huntingdon Valley PA, US |
| Decision | Substantially Equivalent, Sep 30, 2002 |
| Received | Jul 30, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K022512
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.