510(k) K780178 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
TEST SYS. FOR NDNA ANTIBODY DETERM.
| Applicant | Zeus Scientific, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 13, 1978 |
| Received | Feb 3, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K780178
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.