510(k) K781803 ยท GKT Separator, Automated, Blood Cell, Diagnostic
FILTER, EYRPUR DISPOSABLE LEUKOCITE
| Applicant | Metrix Teknika, Inc. MD, US |
| Decision | Substantially Equivalent, Jan 17, 1979 |
| Received | Oct 23, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K781803
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.