510(k) K770663 ยท HCC Device, Biofeedback
FEEDBACK EMG SYSTEM, MODEL PE-L00
| Applicant | Bio-Feedback Systems, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 26, 1977 |
| Received | Apr 7, 1977 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K770663
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.