FDA 510(k) Applications Submitted by Stephanie Anderson

FDA 510(k) Number	Submission Date	Device Name	Applicant
K250824	03/18/2025	Percuflex Ureteral Stent; Percuflex Plus Ureteral Stent; Percuflex Plus SureDrive Steerable Ureteral Stent Set; Contour Ureteral Stent; Contour SureDrive Steerable Ureteral Stent Set; Contour VL Variable Length Ureteral Stent; Contour VL SureDrive Steerab	Boston Scientific Corporation
K201299	05/15/2020	HD Steth	HD Medical, Inc.