# K974346: Starlight Pulsed Diode Array Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Star Medical Technologies, Inc.
- Decided: Jan 16, 1998 after 58 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
No predicates in its family tree.
474 later devices descend from it; 3 cite it directly.
0 of 475 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) PhotoGenica LPIR™: named in the summary without a submission number

## Most influential descendants
- K060448: Lumenis One Family of Systems; Lumenis One. (2006), 297 descendants of its own
- K072564: Alma Lasers Harmony XL Multi-Application Platform (2008), 266 descendants of its own
- K083899: Revlite Q-Switched ND:Yag Laser System (2009), 198 descendants of its own
- K011747: Palomar LC 100 Diode Laser (2001), 174 descendants of its own
- K032846: Spectra Pulsed Diode Laser, Model DR-1 (2003), 173 descendants of its own

## Indications for use
The StarLight™ Pulsed Diode Array Laser System is intended for the treatment of leg veins in Dermatology and Plastic Surgery procedures.

Source page: https://510kreport.com/device/K974346
Methodology: https://510kreport.com/methodology