510(k) K893723 ยท ESD Hearing Aid, Air-Conduction, Prescription
LORI-MODEL L, CANAL IN-THE-EAR INSTRUMENT
| Applicant | Lori Medical Laboratories, Inc., Long Lake MN, US |
| Decision | Substantially Equivalent, Sep 8, 1989 |
| Received | May 17, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893723
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.