ClearanceBrief
510(k) K000125 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

JET PORT PLUS CATHETER SYSTEM

ApplicantClinical Plastic Products SA, Rancho Santa Margarita CA, US
DecisionSubstantially Equivalent, Apr 12, 2000
ReceivedJan 18, 2000
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K000125

DateFirm and productCodeLinked 510(k)
Apr 27, 2015Medical Components, Inc dba MedComp
9F Plastic Dual Port; The port systems are totally implantable vascular access devices. They consist of an injection port, a self-sealing membrane and a detachable catheter. The port systems provide r
Terminated
LJTNone listed

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