# K030692: Power Laser 90

- Pathway: 510(k) (Traditional)
- Applicant: Andi Electromedical Aps
- Decided: Jul 17, 2003 after 134 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: 1 generation back to K010175 (2002). 1 ancestor in all.
65 later devices descend from it; 3 cite it directly.
0 of 67 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)

## Most influential descendants
- K070516: Powerlaser (2007), 63 descendants of its own
- K083595: Ezlase (2009), 58 descendants of its own
- K121286: EPIC 10 (2012), 31 descendants of its own
- K123971: Cynosure 1064NM Diode Laser (2013), 25 descendants of its own
- K170500: SIROLaser Advance+ (2017), 21 descendants of its own

## Indications for use
The POWER LASER 90 is indicated for adjunctive use in the temporary relief of hand and wrist pain associated with Carpal Tunnel Syndrome.

Source page: https://510kreport.com/device/K030692
Methodology: https://510kreport.com/methodology