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CellFX Percutaneous Electrode System (SYS3000)

Page Type
Cleared 510(K)
510(k) Number
K233705
510(k) Type
Traditional
Applicant
Pulse Biosciences, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2024
Days to Decision
109 days
Submission Type
Summary

CellFX Percutaneous Electrode System (SYS3000)

Page Type
Cleared 510(K)
510(k) Number
K233705
510(k) Type
Traditional
Applicant
Pulse Biosciences, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2024
Days to Decision
109 days
Submission Type
Summary