510(k) K880223 ยท ESD Hearing Aid, Air-Conduction, Prescription
MAGIC EAR MODEL MB BEHIND-THE-EAR HEARING AID
| Applicant | Audiotone, Inc., Phoenix AZ, US |
| Decision | Substantially Equivalent, Mar 14, 1988 |
| Received | Jan 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K880223
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.