K231926
- 510(k) number
- K231926
- Device name
- NeuroStar Advanced Therapy System (All previously cleared models)
- Applicant
- Neuronetics, Inc. PA · US
- Product code
- OBP — Transcranial Magnetic Stimulator
- Decision date
- 2024-03-22
- Date received
- 2023-06-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K231926.pdf
Official FDA record: K231926
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.