510(k) K811022 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
ANA TEST KIT
| Applicant | Immuno-Diagnostic Products, Inc. MD, US |
| Decision | Substantially Equivalent, Apr 23, 1981 |
| Received | Apr 15, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811022
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.