510(k) K884871 ยท ESD Hearing Aid, Air-Conduction, Prescription
RESOUND HES, DIGITALLY PROGR., ITE HEARING AID
| Applicant | Resound Corp., Redwood City CA, US |
| Decision | Substantially Equivalent, Feb 22, 1989 |
| Received | Nov 21, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K884871
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.