510(k) K882266 ยท HCC Device, Biofeedback
DIGITAL EMG MONITOR MYOTRON 120
| Applicant | Ats Co., Riverside CA, US |
| Decision | Substantially Equivalent, Aug 15, 1988 |
| Received | May 31, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882266
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.