K231092
- 510(k) number
- K231092
- Device name
- T-SHAPE 2
- Applicant
- B&M S.R.L. Marketing Nel Benessere IT
- Product code
- NUV — Massager, Vacuum, Light Induced Heating
- Decision date
- 2023-09-22
- Date received
- 2023-04-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K231092.pdf
Official FDA record: K231092
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.