510(k) K891693 ยท HCC Device, Biofeedback
AUTOMATED THERAPY SYSTEM
| Applicant | Harding & Harris, Inc., Orem UT, US |
| Decision | Substantially Equivalent, Aug 21, 1989 |
| Received | Mar 22, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891693
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.