# K020463: Depilase Yag Lase Plus Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Depilase Group, Ltd.
- Decided: Feb 27, 2002 after 15 days
- Product code: GEX (Powered Laser Surgical Instrument)
- Device class: 2
- Regulation: 21 CFR 878.4810
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K963094 (1996). 12 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 14 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K990718: Orion Series Surgical  Laser System (SL Seriesq-Switched ND:Yag Configuration), Laserscope (2000) Summary page 2.
- K991798: Acme Medical Aesthetic ND:Yag Laser, Altus Medical (2000) Summary page 2.

## Most influential descendants
- K021650: Athoscan for the Athos Laser Constans Cooling Hand Piece for the Athos Laser (2002), 0 descendants of its own

## Indications for use
The DEPILASE YAG LASE PLUS Laser System is intended for the coagulation and haemostasis of vascular lesions and the removal and permanent reduction of unwanted hair in Fitzpatrick skin types I —VI, including suntanned skin types.

Source page: https://510kreport.com/device/K020463
Methodology: https://510kreport.com/methodology