510(k) K874380 ยท ESD Hearing Aid, Air-Conduction, Prescription
BTE HEARING AID OTICON MODEL E38P
| Applicant | Oticon Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Dec 29, 1987 |
| Received | Oct 26, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K874380
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.