510(k) K890704 ยท ESD Hearing Aid, Air-Conduction, Prescription
BTE HEARING AID OTICON MODEL: E42P
| Applicant | Oticon Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Mar 9, 1989 |
| Received | Feb 10, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K890704
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.