510(k) K790746 ยท HCC Device, Biofeedback
THE BIONIC EXERCISER
| Applicant | Scudder Molner Instruments, Mchenry IL, US |
| Decision | Substantially Equivalent, May 14, 1979 |
| Received | Apr 16, 1979 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K790746
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.