ClearanceBrief
510(k) K101417 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

BABYLANCE HEEL INCISION DEVICE , MODELS BLP50, BLP200, BLN50, BLN200

ApplicantMedipurpose Pte. , Ltd., Alpharetta GA, US
DecisionSubstantially Equivalent, Oct 19, 2010
ReceivedMay 20, 2010
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K101417

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.