510(k) K884400 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
ANTI-NATIVE DNA ANTIBODY TEST (CRITHIDIA LUCILIAE)
| Applicant | Immco Diagnostics, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Nov 4, 1988 |
| Received | Oct 19, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884400
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.