Last synced on 24 May 2024 at 11:04 pm

NeuroStar Advanced Therapy System (All previously cleared models)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231926
510(k) Type
Traditional
Applicant
Neuronetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
266 days
Submission Type
Summary

NeuroStar Advanced Therapy System (All previously cleared models)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231926
510(k) Type
Traditional
Applicant
Neuronetics, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/22/2024
Days to Decision
266 days
Submission Type
Summary