ClearanceBrief
510(k) K222617 ยท QRK Single Use Only Blood Lancet Without An Integral Sharps Injury Prevention Feature

EasyTouch Lancing Device

ApplicantStat Medical Devices, North Miami Beach FL, US
DecisionSubstantially Equivalent, Mar 21, 2023
ReceivedAug 30, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222617

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.