510(k) K083679 ยท IKN Electromyograph, Diagnostic
UROVAL BRS SYSTEM, MODEL BRS01; TELESIS, MODEL PROMO1
| Applicant | Uroval, Minneapolis MN, US |
| Decision | Substantially Equivalent, Sep 11, 2009 |
| Received | Dec 11, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K083679
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.