ClearanceBrief
510(k) K141138 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

SURFLASH SAFETY I.V. CATHETER

ApplicantKofu Factory of Terumo Corp., Elkton MD, US
DecisionSubstantially Equivalent, May 30, 2014
ReceivedMay 2, 2014
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K141138

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.