510(k) K850762 ยท ESD Hearing Aid, Air-Conduction, Prescription
EARETTE HEARING AID OTICON MODEL E32S
| Applicant | Oticon Corp., Somerset NJ, US |
| Decision | Substantially Equivalent, Mar 25, 1985 |
| Received | Feb 25, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K850762
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.