510(k) K874744 ยท ESD Hearing Aid, Air-Conduction, Prescription
OTICON MODEL I50 IN-THE-EAR HEARING AID
| Applicant | Oticon Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Dec 10, 1987 |
| Received | Nov 18, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874744
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.