510(k) K810459 ยท DHX System, Test, Carcinoembryonic Antigen
THREE LEVEL CONTROL SERA
| Applicant | Bd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US |
| Decision | Substantially Equivalent, Aug 3, 1981 |
| Received | Feb 20, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810459
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.