510(k) K943535 ยท HCC Device, Biofeedback
MODEL ME 300 MUSCLE TESTER
| Applicant | Regulatory Strategies, Inc., Eagan MN, US |
| Decision | Substantially Equivalent, Jun 25, 1997 |
| Received | Jul 21, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K943535
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.