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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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