510(k) K870458 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
HISTONES EIA DIAGNOSTIC KIT
| Applicant | Biohytech International, Inc., Chicago IL, US |
| Decision | Substantially Equivalent, Mar 17, 1987 |
| Received | Jan 21, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K870458
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.