510(k) K772219 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
FIAX TEST FOR ANTI-RUBELLA ANTIBODY
| Applicant | Idt, A Division of Whittaker M.A. Bioproducts, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 20, 1978 |
| Received | Dec 5, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K772219
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.