510(k) K942702 ยท ESD Hearing Aid, Air-Conduction, Prescription
DEEP CANAL HEARING INSTRUMENT
| Applicant | Rexton, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, Dec 21, 1994 |
| Received | Jun 8, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942702
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.