K230657
- 510(k) number
- K230657
- Device name
- BTL-99-OC
- Applicant
- BTL Industries, Inc. MA · US
- Product code
- QCI — Transcranial Magnetic Stimulation System For Obsessi
- Decision date
- 2024-02-01
- Date received
- 2023-03-09
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K230657.pdf
Official FDA record: K230657
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.