510(k) K960052 ยท ESD Hearing Aid, Air-Conduction, Prescription
RESOUND PERSONAL HEARING SYSTEM BT2-ES, BT2-EV, & BT241
| Applicant | Resound Corp., Redwood City CA, US |
| Decision | Substantially Equivalent, Mar 12, 1996 |
| Received | Jan 4, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960052
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.