510(k) K974257 ยท ESD Hearing Aid, Air-Conduction, Prescription
RESOUND DIGITAL 2000-BT W/DIGITAL 2000-DF (DIGITAL PROGRAMMER)
| Applicant | Resound Corp., Greeley CO, US |
| Decision | Substantially Equivalent, Dec 12, 1997 |
| Received | Nov 13, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K974257
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.