K232992
- 510(k) number
- K232992
- Device name
- 10THERMA
- Applicant
- Tentech, Inc. KR
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2023-12-20
- Date received
- 2023-09-22
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.3 MB · U.S. public domain
Also available from FDA: K232992.pdf
Official FDA record: K232992
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.