K233010
- 510(k) number
- K233010
- Device name
- Beagank 4T Plus
- Applicant
- Belega, Inc. JP
- Product code
- NFO — Stimulator, Transcutaneous Electrical, Aesthetic Pur
- Decision date
- 2023-11-21
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Neurology
PDFDownload 510(k) SummaryArchived here · 2.7 MB · U.S. public domain
Also available from FDA: K233010.pdf
Official FDA record: K233010
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.