ClearanceBrief
510(k) K072798 ยท LIT Catheter, Angioplasty, Peripheral, Transluminal

VIATRAC 14 PLUS PERIPHERAL DILATION CATHETER

ApplicantAbbott Vascular-Vascular Solutions, Santa Clara CA, US
DecisionSubstantially Equivalent, Jan 31, 2008
ReceivedOct 1, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K072798

DateFirm and productCodeLinked 510(k)
Mar 22, 2010Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Peripheral Dilatation Catheter, Viatrac 14 Plus 5.0mm x 15mm x 80cm, Part Number 1008194-15. Manufactured by Abbott Vascular, Temecula, CA. Indicated to dilate stenosis in the peripheral vasculature
Terminated
LITNone listed

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