ClearanceBrief
510(k) K840197 ยท LFJ Catheter, Subclavian

SINGLE LUMEN SUBCLAVIAN CANNULA

ApplicantShiley, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 25, 1984
ReceivedJan 18, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840197

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.