ClearanceBrief
510(k) K940867 ยท FPA Set, Administration, Intravascular

CONTROL-A-FLO(TM) REGULATOR

ApplicantBaxter Healthcare Corp, Round Lake IL, US
DecisionSubstantially Equivalent, May 5, 1994
ReceivedFeb 23, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K940867

DateFirm and productCodeLinked 510(k)
Jan 11, 2012Baxter Healthcare Corp.
Baxter Interlink System Continu-Flo Solution Set with Control-A-Flo Regulator, 89" (2.3 m), 2 Injection Sites, Male Luer Lock Adapter; an Rx sterile, nonpyrogenic fluid pathway for the administration
Terminated
FPANone listed

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