510(k) K901747 ยท ESD Hearing Aid, Air-Conduction, Prescription
AUDIOTONE ITE HEARING AID MODEL ZG (MIRAGE)
| Applicant | Miracle-Ear, Inc., Minneapolis MN, US |
| Decision | Substantially Equivalent, May 29, 1990 |
| Received | Apr 17, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901747
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.