ClearanceBrief
510(k) K832284 ยท FPA Set, Administration, Intravascular

SOLUTION ADMIN. SET 2C9096 W/10 PVC

ApplicantTravenol Laboratories, S.A., Walker MI, US
DecisionSubstantially Equivalent, Dec 29, 1983
ReceivedJul 13, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K832284

DateFirm and productCodeLinked 510(k)
Nov 16, 2004Baxter Healthcare Corp.
Baxter Clearlink Intravenous (IV) Delivery System; the system consists of solution sets, extension sets and blood sets that have a luer activated valve for IV access, which allows the administration
Terminated
FPANone listed
Aug 21, 2003Baxter Healthcare Corp.
Clearlink System Nitroglycerin Set with DUO-VENT Spike, 60 drops/mL, 105'', PVC Tubing Segment, Luer Activated Valve, Male Luer Lock Adapter, catalog 2C8851; Baxter Healthcare Corporation, Deerfield,
Terminated
FPANone listed

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