510(k) K901388 ยท ESD Hearing Aid, Air-Conduction, Prescription
SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT
| Applicant | Miracle-Ear, Inc., Golden Valley MN, US |
| Decision | Substantially Equivalent, Apr 16, 1990 |
| Received | Mar 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901388
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.