# K953074: Modified Luxar LX-20 Family CO2 Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Luxar Corp.
- Decided: Aug 28, 1995 after 59 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.
407 later devices descend from it; 6 cite it directly.
0 of 408 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K960475: Modified Luxar LX-20 Family CO2 Laser System (1996), 403 descendants of its own
- K991628: Modified LX-20 CO2 Laser System Family, LX-20SA (1999), 377 descendants of its own
- K022060: Lumenis Ultrapulse Encore Carbon Dioxide Surgical Lasers and Delivery Device Accessories (2002), 376 descendants of its own
- K030147: Lumenis Family of Ultrapulse Surgitouch CO2 Surgical Lasers (2003), 323 descendants of its own
- K031795: Reliant Laser System (2003), 318 descendants of its own

Source page: https://510kreport.com/device/K953074
Methodology: https://510kreport.com/methodology