510(k) K063645 ยท BYI Percussor, Powered-Electric
FREQUENCER, MODEL 1001
| Applicant | Dymedso, Inc., Springfield VT, US |
| Decision | Substantially Equivalent, Mar 15, 2007 |
| Received | Dec 7, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063645
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.