510(k) K983712 ยท EWO Audiometer
AMPLAID A311 SERIES
| Applicant | Amplifon S.P.A., Deer Field IL, US |
| Decision | Substantially Equivalent, Jan 12, 1999 |
| Received | Oct 21, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K983712
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.