510(k) K082634 ยท LXV Apparatus, Vestibular Analysis
VERTIGONE BPPV GOGGLE
| Applicant | Vertigone, Inc., Woodlands TX, US |
| Decision | Substantially Equivalent, Apr 7, 2009 |
| Received | Sep 10, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082634
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.