ClearanceBrief
510(k) K244036 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Heel Incision Safety Lancet (SteriHeel 2)

ApplicantSteriLance Medical (Suzhou), Inc., Suzhou, CN
DecisionSubstantially Equivalent, Feb 26, 2025
ReceivedDec 30, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K244036

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.