510(k) K782048 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
TEST KIT, IIF-ANA
| Applicant | Medica Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 17, 1979 |
| Received | Dec 8, 1978 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K782048
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.