ClearanceBrief
510(k) K922434 ยท LJT Port & Catheter, Implanted, Subcutaneous, Intravascular

A PORT IMPLANTABLE VASCULAR ACCESS SYSTEM LINE EXT

ApplicantTherex Corp., Walpole MA, US
DecisionSubstantially Equivalent, Nov 6, 1992
ReceivedMay 22, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922434

DateFirm and productCodeLinked 510(k)
Dec 19, 2006Arrow International Inc
Implantable Vascular Access system --Infusion Ports with Silicone Rubber Catheter. Latex-free A Port. 9 Fr. Introducer Kit. Ref. Product No. AP-06018.
Terminated
LJTNone listed

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