# K151793: InMode RF System

- Pathway: 510(k) (Traditional)
- Applicant: Inmode MD, Ltd.
- Decided: Feb 19, 2016 after 233 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 18 generations back to K943450 (1995). 104 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 106 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K130689: Symphony RF Generator, Thermigen, Inc. (2013) Summary page 4.

## Most influential descendants
- K163190: InMode RF System (2016), 0 descendants of its own

## Indications for use
The InMode RF System is indicated for use in dermatological and general surgical procedures for electro-coagulation and hemostasis.

Source page: https://510kreport.com/device/K151793
Methodology: https://510kreport.com/methodology