510(k) K902179 ยท ESD Hearing Aid, Air-Conduction, Prescription
VISTA - MODELS V12, V20, V23, V38, ITE HEARING AID
| Applicant | Vista Laboratories, Inc., Centralia WA, US |
| Decision | Substantially Equivalent, Aug 10, 1990 |
| Received | May 15, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K902179
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.