510(k) K832122 ยท HCC Device, Biofeedback
ENRAF NONIVS2 CHANNEL EMG/TEMP. FEED
| Applicant | Fluidotherapy Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Aug 12, 1983 |
| Received | Jun 30, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K832122
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.