510(k) K892114 ยท HCC Device, Biofeedback
ELECTRO-PHYSIO-FEEDBACK-XRROID* SYSTEM
| Applicant | Eclosion, Inc., Denver CO, US |
| Decision | Substantially Equivalent, Oct 13, 1989 |
| Received | Mar 30, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892114
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.