Pulse Biosciences Submits 510(K) to U.S. FDA for CellFX(TM) System

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More Recent News About Pulse Biosciences Inc

Pulse Biosciences Schedules First Quarter 2024 Financial Results Conference Call for May 7, 2024
Pulse Biosciences Reports Business Updates and Fourth Quarter & Full Year 2023 Financial Results
Pulse Biosciences Announces Plans to Initiate a Rights Offering
Pulse Biosciences Schedules Fourth Quarter & Full Year 2023 Financial Results Conference Call for March 28, 2024
Pulse Biosciences Announces FDA 510(k) Clearance for its CellFX® nsPFA(TM) Percutaneous Electrode System
Pulse Biosciences Announces Positive 60-Day Follow-Up Evaluations for Initial Patients treated in the CellFX® nsPFA(TM) 360° Cardiac Catheter First-in-Human Feasibility Study
Pulse Biosciences Announces Preliminary Findings from its CellFX nsPFA 360 Cardiac Catheter First-In-Human Feasibility Study to be Featured in Podium Presentation at the AF Symposium
Pulse Biosciences Files 510(k) Submission with U.S. FDA for its CellFX® nsPFA(TM) Cardiac Clamp

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