510(k) Report

Devices descending from K172090

8 later devices reach GuideLiner V3 Catheter through their predicates, nearest generation first.

GenerationNumberDeviceApplicantDecidedOwn descendantsRecalls
+1K220691LiquID 061 Guide Catheter Extension, LiquID 071 Guide Catheter ExtensionSeigla Medical, Inc.20221—
+1K210110GuidionImds Operations B.V.20211—
+1K183353Telescope Guide Extension CatheterMedtronic, Inc.20193—
+2K252390Telescope Guide Extension CatheterMedtronic, Ireland20250—
+2K242337FlowGuide (FG60F); GuidionShort (GS60F)Imds Operations B.V.20250—
+2K243691LiquID .051 LP Guide Catheter ExtensionSeigla Medical, Inc.20250—
+2K242276CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)Vantis Vascular, Inc.20241—
+3K262817CrossFAST Integrated Microcatheter Advanced Delivery SystemVantis Vascular, Inc.20260—