510(k) K073636 ยท KLW Masker, Tinnitus
TINNITUS SOUND GENERATOR MODULE
| Applicant | Gn Resound A/S, Ballerup, DK |
| Decision | Substantially Equivalent, Mar 13, 2008 |
| Received | Dec 26, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073636
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.