510(k) K842354 ยท HCC Device, Biofeedback
EMG MODEL 133
| Applicant | Calnor of EL Paseo, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jul 17, 1984 |
| Received | May 7, 1984 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K842354
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.