510(k) K881164 ยท HCC Device, Biofeedback
LEUNOMED RFB 5000
| Applicant | Hemodynamics, Inc., Boca Raton FL, US |
| Decision | Substantially Equivalent, Apr 24, 1989 |
| Received | Mar 18, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K881164
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.