510(k) K895635 ยท HCC Device, Biofeedback
MYOSYSTEM 1000 ELECTROMYOGRAPH
| Applicant | Noraxon USA, Inc., Scottsdale AZ, US |
| Decision | Substantially Equivalent, Apr 19, 1990 |
| Received | Sep 19, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K895635
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.