K241733
- 510(k) number
- K241733
- Device name
- HEBE (NP0000763)
- Applicant
- Novasonix Technology S.L. ES
- Product code
- PBX — Massager, Vacuum, Radio Frequency Induced Heat
- Decision date
- 2025-04-16
- Date received
- 2024-06-17
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 3.0 MB · U.S. public domain
Also available from FDA: K241733.pdf
Official FDA record: K241733
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.