ClearanceBrief
510(k) K122544 ยท FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days

TERUMO SURFLASH SAFETY I.V. CATHETER

ApplicantTerumo Corporation, Yamanashi, JP
DecisionSubstantially Equivalent, Sep 5, 2012
ReceivedAug 21, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K122544

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.