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FDA 510(k) Applications Submitted by Cassie Clark
FDA 510(k) Number
Submission Date
Device Name
Applicant
K230453
02/21/2023
OptiCrossTM HD Coronary Imaging Catheter, OptiCrossTM 6 HD Coronary Imaging Catheter
Boston Scientific Corporation
K222568
08/24/2022
OptiCrossÖ 18 Peripheral Imaging Catheter
Boston Scientific Corporation
K213593
11/12/2021
OptiCross, OptiCross HD, OptiCross 6, OptiCross 6 HD
Boston Scientific Corporation
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