510(k) K880273 ยท ESD Hearing Aid, Air-Conduction, Prescription
WIDEX HEARING AID MODEL C1
| Applicant | Widex Hearing Aid Co., Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, Mar 14, 1988 |
| Received | Jan 22, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880273
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.