510(k) K884113 ยท ESD Hearing Aid, Air-Conduction, Prescription
HEARING AID WIDEX BTE
| Applicant | Widex Hearing Aid Co., Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, Dec 19, 1988 |
| Received | Sep 29, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884113
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.