ClearanceBrief
510(k) K840760 ยท FPA Set, Administration, Intravascular

HARVARD ANTI-REFLUX Y-SET

ApplicantC.R. Bard, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 5, 1984
ReceivedFeb 23, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K840760

DateFirm and productCodeLinked 510(k)
Aug 30, 2005Baxter Healthcare Corp.
Baxter Tamper Resistant Anti-Siphon Combination Set, 101'', product code 2L3507; An Rx sterile, nonpyrogenic fluid pathway, 101'', 2.5 mL Vol., with male Luer Lock adapter; Baxter Healthcare Corporati
Terminated
FPANone listed

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