ClearanceBrief
510(k) K924721 ยท FPA Set, Administration, Intravascular

BAXTER SOLUTION ADMINISTRATION SETS

ApplicantBaxter Healthcare Corp, Round Lake IL, US
DecisionSubstantially Equivalent, Jul 20, 1993
ReceivedSep 21, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K924721

DateFirm and productCodeLinked 510(k)
Mar 24, 2006Baxter Healthcare Corp.
Baxter Interlink System Extension Set with Standard Bore 4-Way Stopcock Manifold Extension Set and Minivolume Extension Set, product code 3C0071; An Rx sterile, nonpyrogenic fluid pathway; extension s
Terminated
FMGNone listed
Aug 21, 2003Baxter Healthcare Corp.
Interlink System Vented Nitroglycerin Set, 104 '', PVC Tubing Segment, Injection Site, Male Luer Lock Adapter, catalog 2C7551; Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Terminated
FPANone listed
Aug 21, 2003Baxter Healthcare Corp.
Baxter Vented Nitroglycerin Set, 105'', PVC Tubing Segment, Injeciton Site, Male Luer Lock Adapter, catalog 2C7552; Baxter Healthcare Corporation, Deerfield, IL 60015 USA
Terminated
FPANone listed
Aug 21, 2003Baxter Healthcare Corp.
Baxter Y-Type Blood/Solution Set with Pressure Pump, 10 drops/mL, 99'', 170 to 260 Micron Filter,Large Standard Blood Filter, 2 Injection Sites, Male Luer Lock Adapter, catalog 2C6723; Baxter Healthca
Terminated
KSBNone listed
Feb 6, 2003Baxter Healthcare Corp.
Baxter Minivolume Extension Set with 0.22 Micron High Pressure Pediatric Filter, catalog 2C5693; Baxter Healthcare Corporation, Deerfield, IL 60015; 48 units per case
Terminated
FPANone listed

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