ClearanceBrief
510(k) K001162 ยท FMK Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

GOLDFINGER DEVICE

ApplicantMali-Tech , Ltd., Ginot Shomron 44853, IL
DecisionSubstantially Equivalent, Aug 9, 2000
ReceivedApr 10, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K001162

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.