# K073300: Milesman Premium

- Pathway: 510(k) (Traditional)
- Applicant: Milesman S.L.
- Decided: Dec 4, 2007 after 11 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: 1 generation back to K003614 (2001). 1 ancestor in all.
6 later devices descend from it; 2 cite it directly.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K003614: Lightsheer Pulsed Diode Array Laser System, Coherent Star (2001) Summary page 1.

## Most influential descendants
- K120622: Palomar Vectus Laser (2012), 4 descendants of its own
- K193426: Elite iQ (2020), 1 descendant of its own
- K162765: Venus Velocity Diode Laser System (2017), 1 descendant of its own
- K240396: Elite iQ PRO (M122K1) (2024), 0 descendants of its own
- K203804: Global Med Systems Milesman Compact Laser (2021), 0 descendants of its own

## Indications for use
The Milesman Premium Pulsed Diode Array Laser System is intended for use in general and plastic surgery and dermatology procedures for the treatment of vascular lesions, such as angiomas, hemangiomas, telangiectasia and other benign vascular lesions and treatment for pseudofolliculitis barbae. The Milesman Premium is also used for removal of unwanted hair, permanent hair reduction and the treatment of benign pigmented lesions and leg veins in all skin types (Fitzpatrick I-VI), including tanned skin.

Source page: https://510kreport.com/device/K073300
Methodology: https://510kreport.com/methodology