510(k) K081602 ยท LXV Apparatus, Vestibular Analysis
DIZZYFIX
| Applicant | Clearwater Clinical Limited, Calgary, Alberta, CA |
| Decision | Substantially Equivalent, Sep 19, 2008 |
| Received | Jun 6, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K081602
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.