ClearanceBrief
510(k) K925058 ยท FPA Set, Administration, Intravascular

BARD AMBU PUMP SPIK TUB SET PACRET PROVID PUMP SET

ApplicantC.R. Bard, Inc., North Reading MA, US
DecisionSubstantially Equivalent, Aug 3, 1993
ReceivedOct 6, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925058

DateFirm and productCodeLinked 510(k)
Jun 29, 2011Baxter Healthcare Corp.
Baxter Solution Set for Epidural Use, 110" (2.8 m), Male Luer Lock Adapter; a sterile, single use, nonpyrogenic fluid pathway for use with 6200 and 6300 series Flo-Gard Volumetric Infusion Pumps; Baxt
Terminated
FPANone listed

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