510(k) K802299 ยท DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control
K/K (ASMA/ANA) UNIVERSAL BIOPAK
| Applicant | Bioware Products, Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 29, 1981 |
| Received | Sep 19, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K802299
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.