510(k) K922270 ยท HCC Device, Biofeedback
PHYSIOTECH 4000 OR NORODYN 8000
| Applicant | Myo-Tronics, Inc., Seattle WA, US |
| Decision | Substantially Equivalent, Sep 2, 1994 |
| Received | May 14, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K922270
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.