K233742
- 510(k) number
- K233742
- Device name
- CloudTMS Edge for OCD
- Applicant
- Teleemg, LLC CA · US
- Product code
- QCI — Transcranial Magnetic Stimulation System For Obsessi
- Decision date
- 2023-12-22
- Date received
- 2023-11-22
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K233742.pdf
Official FDA record: K233742
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.