510(k) K883915 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control
AUTOANTIBODY TEST SYSTEM (MOUSE KIDNEY/STOMACH)
| Applicant | Immco Diagnostics, Inc., Buffalo NY, US |
| Decision | Substantially Equivalent, Oct 19, 1988 |
| Received | Sep 16, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K883915
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.