ClearanceBrief
510(k) K133298 ยท EKX Handpiece, Direct Drive, Ac-Powered

ENDO SMART

ApplicantMeta Biomed, Inc., Mt. Airy MD, US
DecisionSubstantially Equivalent, Sep 19, 2014
ReceivedOct 25, 2013
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K133298

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.