Skip to content
510(k)
Report
Search FDA device records
/
Guides
Tracker
Methodology
Get a report
Report
510(k) Report
›
K112571
›
Descendants
Devices descending from K112571
2 later devices reach XL Extraction Catheter through their predicates, nearest generation first.
Generation
Number
Device
Applicant
Decided
Own descendants
Recalls
+1
K173266
Octane aspiration system
Vascular Solutions, Inc.
2017
1
—
+2
K182232
Octane Mechanical Thrombectomy System
Vascular Solutions, Inc.
2018
0
—