510(k) K885128 ยท ESD Hearing Aid, Air-Conduction, Prescription
WIDEX BTE HEARING AID MODEL Q8
| Applicant | Widex Hearing Aid Co., Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, Mar 1, 1989 |
| Received | Dec 12, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885128
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.