# K170709: CURVE Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Yolo Medical, Inc.
- Decided: Jun 6, 2017 after 90 days
- Product code: OLI (Fat Reducing Low Level Laser)
- Device class: 2
- Regulation: 21 CFR 878.5400
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 17 generations back to K943450 (1995). 63 ancestors in all.
No later device cites it as a predicate yet.
0 of 64 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K143741: Lipofina Laser System, Yolo Medical, Inc. (2015) Summary page 5.

## Indications for use
The CURVE Laser System is indicated for non-invasive aesthetic treatment for the temporary reduction in circumference of the waist.

Source page: https://510kreport.com/device/K170709
Methodology: https://510kreport.com/methodology