510(k) K960804 ยท ESD Hearing Aid, Air-Conduction, Prescription
MIRACLE EAR & AUDIOTONE MODEL ITE/ITC/CIC
| Applicant | Miracle-Ear, Inc., Golden Valley MN, US |
| Decision | Substantially Equivalent, Apr 5, 1996 |
| Received | Feb 28, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960804
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.