ClearanceBrief
510(k) K964154 ยท KRA Catheter, Continuous Flush

SEGUE INFUSION CATHETER

ApplicantInterventional Innovations Corp., St. Paul MN, US
DecisionSubstantially Equivalent, Jan 14, 1997
ReceivedOct 16, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K964154

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.