510(k) K953884 ยท EWO Audiometer
PROPHET
| Applicant | Qualitone, Minneapolis MN, US |
| Decision | Substantially Equivalent, Oct 27, 1995 |
| Received | Aug 17, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K953884
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.