510(k) K990352 ยท GKZ Counter, Differential Cell
COULTER AC T DIFF 2 ANALYZER
| Applicant | Coulter Corp., Miami FL, US |
| Decision | Substantially Equivalent, Apr 1, 1999 |
| Received | Feb 5, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990352
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 21, 2004 | Beckman Coulter Inc ACT diff 2 Analyzer
(Automated differential cell counter) Terminated |
GKZ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.