510(k) K803099 ยท HCC Device, Biofeedback
BIOFEEDBACK BIO 80
| Applicant | Bimed, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Mar 2, 1981 |
| Received | Dec 8, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K803099
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.