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NeuroStar Advanced Therapy System (Version 3.8)

Page Type
Cleared 510(K)
510(k) Number
K233621
510(k) Type
Special
Applicant
Neuronetics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
30 days
Submission Type
Summary

NeuroStar Advanced Therapy System (Version 3.8)

Page Type
Cleared 510(K)
510(k) Number
K233621
510(k) Type
Special
Applicant
Neuronetics
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2023
Days to Decision
30 days
Submission Type
Summary