K233621
- 510(k) number
- K233621
- Device name
- NeuroStar Advanced Therapy System (Version 3.8)
- Applicant
- Neuronetics PA · US
- Product code
- OBP — Transcranial Magnetic Stimulator
- Decision date
- 2023-12-13
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.4 MB · U.S. public domain
Also available from FDA: K233621.pdf
Official FDA record: K233621
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.