510(k) K972959 ยท GWF Stimulator, Electrical, Evoked Response
AMPLAID MK22
| Applicant | Amplifon S.P.A., Deer Field IL, US |
| Decision | Substantially Equivalent, Feb 6, 1998 |
| Received | Aug 11, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K972959
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.