ClearanceBrief
510(k) K895858 ยท LYY Latex Patient Examination Glove

CLP ELEVATED LIPID CONTROL

ApplicantCreative Laboratory Products, Inc., Indianapolis IN, US
DecisionSubstantially Equivalent, Jan 26, 1990
ReceivedOct 3, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895858

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.