Last synced on 1 March 2024 at 11:05 pm

NeuroStar Advanced Therapy System (Version 3.8)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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