# K063574: Luminex LL Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Medical Laser Systems, Inc.
- Decided: Jan 29, 2007 after 61 days
- Product code: NHN (Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy)
- Device class: 2
- Regulation: 21 CFR 890.5500
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K010175 (2002). 5 ancestors in all.
No later device cites it as a predicate yet.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K010175: Microlight 830 Laser System, Microlight Corporation of America (2002) Summary page 2.
- K020657: Acculaser Pro Low Level Laser Therapy Device, Acculaser, Inc. (2002) Summary page 2.
- K034009: LAPEX 2000, Meridian Co., Ltd. (2005) Summary page 2.

## Indications for use
Adjunctive use in the temporary relief of hand and wrist pain associated with Carpal Tunnel Syndrome

Source page: https://510kreport.com/device/K063574
Methodology: https://510kreport.com/methodology