510(k) K951379 ยท ESD Hearing Aid, Air-Conduction, Prescription
RESOUND PERSONAL HEARING SYSTEM MODELS ED3A & ED3A/S W/REMONTE CONTROL OPTION
| Applicant | Resound Corp., Redwood City CA, US |
| Decision | Substantially Equivalent, Apr 27, 1995 |
| Received | Mar 27, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951379
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.