K232172
- 510(k) number
- K232172
- Device name
- BTL-785BNF Handpiece
- Applicant
- BTL Industries, Inc. MA · US
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2023-09-18
- Date received
- 2023-07-21
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K232172.pdf
Official FDA record: K232172
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.