510(k) K963202 ยท HCC Device, Biofeedback
MEGA ME 3000 PROFESSIONAL MUSCLE TESTER
| Applicant | Mega Electronics , Ltd., Eagan MN, US |
| Decision | Substantially Equivalent, May 19, 1997 |
| Received | Aug 15, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K963202
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.