ClearanceBrief
510(k) K770431 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

CATHETER, TWO STAGE VENOUS RETURN

Applicant3M Health Care, Sarns, Mchenry IL, US
DecisionSubstantially Equivalent, Mar 16, 1977
ReceivedMar 7, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770431

DateFirm and productCodeLinked 510(k)
Jul 23, 2014Terumo Cardiovascular Systems Corporation
Sarns Two-stage Venous Return Cannulae 32/40 & 36/51 Fr with 1/2" & 3/8" flare or connector Product Usage: The Venous Return Cannula is indicated for venous drainage during cardiopulmonary bypass sur
Terminated
DWFNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.