510(k) K955878 ยท ESD Hearing Aid, Air-Conduction, Prescription
WIDEX MODEL SENSO DIGITAL (C8)
| Applicant | Widex Hearing Aid Co., Inc., Long Island City NY, US |
| Decision | Substantially Equivalent, Feb 12, 1996 |
| Received | Dec 28, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K955878
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.