510(k) K951350 ยท HCC Device, Biofeedback
MUSCLESENSE ELECTROMYOGRAPHY DEVICE
| Applicant | Smith and Nephew Donjoy, Inc., Carsbad CA, US |
| Decision | Substantially Equivalent, Jun 23, 1995 |
| Received | Mar 24, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951350
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.