510(k) K812179 ยท HCC Device, Biofeedback
LIFE-TECH #1753 BIOFEEDBACK TRAINER
| Applicant | Life-Tech Instruments, Inc., Walker MI, US |
| Decision | Substantially Equivalent, Aug 25, 1981 |
| Received | Aug 3, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K812179
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.