510(k) K760206 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
TEST, DETECTION, ANTINUCLEAR ANTIBODIES
| Applicant | Intl. Diagnostic Technology, Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 3, 1976 |
| Received | Jul 9, 1976 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K760206
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.