K252963
- 510(k) number
- K252963
- Device name
- BTL-899TT
- Applicant
- BTL Industries, Inc. MA · US
- Product code
- IMJ — Diathermy, Shortwave, For Use In Applying Therapeuti
- Decision date
- 2026-06-12
- Date received
- 2025-09-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Physical Medicine
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K252963.pdf
Official FDA record: K252963
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.