510(k) K904181 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control
ANTI-GBM ANTIBODIES QUANTITATIVE KIT
| Applicant | Biochemical Diagnostic, Inc., Sweden, SE |
| Decision | Substantially Equivalent, Sep 10, 1991 |
| Received | Sep 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K904181
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.