ClearanceBrief
510(k) K983413 ยท EKX Handpiece, Direct Drive, Ac-Powered

MODEL MS-1 HANDPIECE

ApplicantParkell, Inc., Farmingdale NY, US
DecisionSubstantially Equivalent, Dec 21, 1998
ReceivedSep 28, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983413

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.