510(k) K972487 ยท HCC Device, Biofeedback
EMG RETRAINER
| Applicant | Chattanooga Group, Inc., Hixson TN, US |
| Decision | Substantially Equivalent, Sep 26, 1997 |
| Received | Jul 2, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972487
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.