510(k) K992444 ยท GKZ Counter, Differential Cell
MODIFICATION OF: CELL-DYN 1200 SYSTEM
| Applicant | Abbott Laboratories, Santa Clara CA, US |
| Decision | Substantially Equivalent, Sep 24, 1999 |
| Received | Jul 22, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K992444
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.