510(k) K811261 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control
ANTI-SKIN ANTIBODY TEST SYSTEM
| Applicant | Zeus Scientific, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 12, 1981 |
| Received | May 6, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K811261
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.