510(k) K953495 ยท DBL Multiple Autoantibodies, Indirect Immunofluorescent, Antigen, Control
EIA KIT FOR THE DETECTION OF GBM ANTIBODIES
| Applicant | Scimedx Corp., Denvill NJ, US |
| Decision | Substantially Equivalent, Apr 10, 1996 |
| Received | Jul 26, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953495
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.