510(k) Report

Devices descending from K112082

12 later devices reach Guideliner V2 Catheter through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K172090GuideLiner V3 CatheterVascular Solutions, Inc.20178—
+1K161901TrapLiner catheterVascular Solutions, Inc.20171—
+1K120707Switch-IT CatheterVascular Solutions, Inc.20120—
+2K220691LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter ExtensionSeigla Medical, Inc.20221—
+2K210110GuidionImds Operations B.V.20211—
+2K183353Telescope Guide Extension CatheterMedtronic, Inc.20193—
+2K180088TrapLiner catheterVascular Solutions, Inc.20180—
+3K252390Telescope Guide Extension CatheterMedtronic, Ireland20250—
+3K242337FlowGuide (FG60F); GuidionShort (GS60F)Imds Operations B.V.20250—
+3K243691LiquID .051 LP Guide Catheter ExtensionSeigla Medical, Inc.20250—
+3K242276CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)Vantis Vascular, Inc.20241—
+4K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.20260—