ClearanceBrief
510(k) K840175 ยท DQY Catheter, Percutaneous

DOUBLE LUMEN INFUSION CATHETERS

ApplicantMedical Components, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 10, 1984
ReceivedJan 17, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840175

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.