510(k) K013253 ยท KLW Masker, Tinnitus
HISONIC-TRD TINNITUS RELIEF DEVICE
| Applicant | Hearing Innovations, Inc., Washington, D.C. DC, US |
| Decision | Substantially Equivalent, Apr 5, 2002 |
| Received | Sep 28, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013253
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.