510(k) K922838 ยท HCC Device, Biofeedback
NORODYN 2000 ELECTROMYOGRAPH
| Applicant | Noromed, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 22, 1993 |
| Received | Jun 12, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922838
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.