FDA 510(k) Applications Submitted by Pulse Biosciences, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K211444 05/10/2021 CellFX System Pulse Biosciences, Inc.
K221671 06/09/2022 CellFX« System Pulse Biosciences, Inc.
K222075 07/14/2022 CellFX System Pulse Biosciences, Inc.
K213674 11/22/2021 CellFX System Pulse Biosciences, Inc.
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.
K203299 11/09/2020 CellFX System Pulse Biosciences, Inc.


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