510(k) K970051 ยท HCC Device, Biofeedback
MUSCLESENSE II CLINICAL ELECTROMYOGRAPHY DEVICE
| Applicant | Smith and Nephew Donjoy, Inc., Carsbad CA, US |
| Decision | Substantially Equivalent, Jul 10, 1997 |
| Received | Jan 7, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970051
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.