510(k) K091000 ยท LXJ Interactive Rehabilitation Exercise Devices
KNEEKG
| Applicant | Emovi, Montreal, Quebec, CA |
| Decision | Substantially Equivalent, Oct 26, 2009 |
| Received | Apr 8, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091000
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.