510(k) K950693 ยท ESD Hearing Aid, Air-Conduction, Prescription
MIRACLE-EAR MODEL PM1/PM2 PROGRAMMABLE HEARING AID
| Applicant | Miracle-Ear, Inc., Golden Valley MN, US |
| Decision | Substantially Equivalent, Mar 31, 1995 |
| Received | Feb 14, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950693
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.