510(k) K913360 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control
ANTI-RETICULIN ANTIBODY (ARA) TEST
| Applicant | Immco Diagnostics, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Sep 26, 1994 |
| Received | Jul 29, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K913360
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.