K260691
- 510(k) number
- K260691
- Device name
- BTL-699
- Applicant
- BTL Industries, Inc. MA · US
- Product code
- OBP — Transcranial Magnetic Stimulator
- Decision date
- 2026-08-23
- Date received
- 2026-03-03
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K260691.pdf
Official FDA record: K260691
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.