510(k) K810881 ยท HCC Device, Biofeedback
EMG 3510/EMG 3510D MYOFEEDBACK MONITORS
| Applicant | Atlas Researches , Ltd., Mchenry IL, US |
| Decision | Substantially Equivalent, May 27, 1981 |
| Received | Mar 31, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810881
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.