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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