# K010372: Lightlas 532 Photocoagulator

- Pathway: 510(k) (Traditional)
- Applicant: Lightmed Corp.
- Decided: Aug 22, 2001 after 196 days
- Product code: HQF (Laser, Ophthalmic)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
9 later devices descend from it; 1 cites it directly.
0 of 10 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
- K021696: 20G Sma Laser Fiber, Model LF20; 25G Sma Laser Fiber, Model LF25 (2002), 8 descendants of its own
- K050807: 20G Sma Laser Fiber, Model LF100 (2005), 6 descendants of its own
- K121187: Katalyst Laser Probes, Katalyst Illuminated Laser Probes (2012), 5 descendants of its own
- K142830: Ophthalmed Bending Laser Probes (2015), 2 descendants of its own
- K191846: MAXReach Laser Probe (2019), 1 descendant of its own

## Recalls of this device
- Nov 11, 2003 · Not classified · Z-0228-04: Firm needed to include calibration procedures in user guide.

Source page: https://510kreport.com/device/K010372
Methodology: https://510kreport.com/methodology