510(k) K960680 ยท ESD Hearing Aid, Air-Conduction, Prescription
RESOUND PERSONAL HEARING SYSTEMS EDR ENCORE SERIES MODELS EDR-E, EDR-ES, EDR-EV, & EDR-P1
| Applicant | Resound Corp., Redwood City CA, US |
| Decision | Substantially Equivalent, Apr 10, 1996 |
| Received | Feb 20, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960680
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.