510(k) K801233 ยท GKT Separator, Automated, Blood Cell, Diagnostic
CELLTRIFUGE II
| Applicant | Travenol Laboratories, S.A., Mchenry IL, US |
| Decision | Substantially Equivalent, Oct 31, 1980 |
| Received | May 27, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K801233
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.