510(k) K063872 ยท GYD Transducer, Tremor
KINESIA
| Applicant | Cleveland Medical Devices, Inc., Cleveland OH, US |
| Decision | Substantially Equivalent, Apr 6, 2007 |
| Received | Dec 29, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063872
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.