# K942622: Laseaway Q-Switched ND:Yag Laser System

- Pathway: 510(k) (Traditional)
- Applicant: Mdi, Inc.
- Decided: Mar 24, 1995 after 295 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.
746 later devices descend from it; 1 cites it directly.
0 of 747 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K970808: Medlite IV Q-Switched, Frequency Doubled, ND:Yag Laser (1997), 745 descendants of its own
- K033946: Lovely System (2004), 737 descendants of its own
- K033251: The Friendlylight ND: Yag Lasers (2004), 519 descendants of its own
- K042000: Modified MSQ Family of Lovely Light/Laser Systems (2004), 517 descendants of its own
- K042630: Revlight Skin Care System (2005), 402 descendants of its own

Source page: https://510kreport.com/device/K942622
Methodology: https://510kreport.com/methodology