ClearanceBrief
510(k) K160660 ยท DQO Catheter, Intravascular, Diagnostic

Medline Waste Station

ApplicantMedline Industries, Inc., Mundelein IL, US
DecisionSubstantially Equivalent, Jan 19, 2017
ReceivedMar 8, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160660

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.