FDA 510(k) Applications Submitted by Melissa Schneider

FDA 510(k) Number Submission Date Device Name Applicant
K240366 02/06/2024 EPòXTÖ Unidirectional Steerable Diagnostic Catheter; Dynamic TipÖ Unidirectional Steerable Diagnostic Catheter; Dynamic XTÖ Unidirectional Steerable Diagnostic Catheter Boston Scientific Corporation
K220796 03/18/2022 IntellaMap Orion High Resolution Mapping Catheter Boston Scientific Corporation


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