510(k) K971740 ยท GWF Stimulator, Electrical, Evoked Response
AMPLAID MK12
| Applicant | Amplifon S.P.A., Deer Field IL, US |
| Decision | Substantially Equivalent, Mar 16, 1998 |
| Received | May 12, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K971740
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.