510(k) K832333 ยท HCC Device, Biofeedback
FEEDBACK EMG SYSTEM PE-020
| Applicant | Bio-Feedback Systems, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Sep 1, 1983 |
| Received | Jul 18, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832333
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.