510(k) K071973 ยท LXV Apparatus, Vestibular Analysis
EPLEY OMNIAX
| Applicant | Vesticon, Portland OR, US |
| Decision | Substantially Equivalent, Jun 20, 2008 |
| Received | Jul 17, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K071973
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.