ClearanceBrief
510(k) K951814 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

TRIUMPH-1 PORT

ApplicantHorizon Medical Products, Inc., Atlanta GA, US
DecisionSubstantially Equivalent, Aug 29, 1995
ReceivedApr 18, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951814

DateFirm and productCodeLinked 510(k)
Nov 17, 2010Angiodynamics, INC
Triumph-1, AngioDynamics, Inc., One Horizon Way, Manchester, GA 31816.
Terminated
FRNNone listed

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