510(k) K892333 ยท ESD Hearing Aid, Air-Conduction, Prescription
REXTON RX12PP, RX20PP & RX34PP IN-THE-EAR HEAR AID
| Applicant | Rexton, Inc., Plymouth MN, US |
| Decision | Substantially Equivalent, May 19, 1989 |
| Received | Apr 5, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K892333
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.