K233642
- 510(k) number
- K233642
- Device name
- InMode RF System
- Applicant
- InMode , Ltd. IL
- Product code
- GEI — Electrosurgical, Cutting & Coagulation & Accessories
- Decision date
- 2024-03-20
- Date received
- 2023-11-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K233642.pdf
Official FDA record: K233642
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.