FDA 510(k) Applications Submitted by Aniket Khakhadiya

FDA 510(k) Number Submission Date Device Name Applicant
K222340 08/03/2022 Chartis Precision Catheter Pulmonx Corporation
K193126 11/12/2019 HI-TORQUE InfilTrac Guide Wire Family Abbott Vascular
K173795 12/14/2017 HI-TORQUE TurnTrac Guide Wire Family Abbott Vascular


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