FDA 510(k) Applications Submitted by Uyen Mai

FDA 510(k) Number Submission Date Device Name Applicant
K240782 03/21/2024 CellFX Percutaneous Electrode System (SYS3000); CellFX Percutaneous Electrode, 13G (CPE013); CellFX Percutaneous Electrode, 18G (CPE018) Pulse Biosciences, Inc.
K233705 11/20/2023 CellFX Percutaneous Electrode System (SYS3000) Pulse Biosciences, Inc.


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