510(k) K832383 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
IDT ANA STIQ ASSAY
| Applicant | Intl. Diagnostic Technology, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 31, 1983 |
| Received | Jul 19, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832383
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.