510(k) K902559 ยท ESD Hearing Aid, Air-Conduction, Prescription
CUSTOM IN-THE-EAR HEARING AID OTICON MODEL: P
| Applicant | Oticon Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Jul 9, 1990 |
| Received | Jun 11, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902559
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.