FDA 510(k) Applications Submitted by Tijana Prodanovic

FDA 510(k) Number Submission Date Device Name Applicant
K234046 12/21/2023 WallFlex Colonic Stent System with Anchor Lock Delivery System; WallFlex Duodenal Stent System with Anchor Lock Delivery System; WallFlex Colonic Soft Stent System with Anchor Lock Delivery System; WallFlex Duodenal Soft Stent System with Anchor Lock Deli Boston Scientific Corporation


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