510(k) K100749 ยท BYI Percussor, Powered-Electric
FREQUENCER MODEL V2X
| Applicant | Dymedso, Inc., Springfield VT, US |
| Decision | Substantially Equivalent, Aug 31, 2010 |
| Received | Mar 16, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K100749
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.