# K011355: Biolight PCD

- Pathway: 510(k) (Traditional)
- Applicant: Biolight International AB
- Decided: Jan 17, 2002 after 259 days
- Product code: ILY (Lamp, Infrared, Therapeutic Heating)
- 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
No predicates in its family tree.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K051681: Dermillume Red, Model HR1000 (2005), 3 descendants of its own
- K081570: DPL Therapy System (2008), 1 descendant of its own
- K150554: NuBrilliance Light Pain Therapy (2015), 0 descendants of its own
- K070690: The Life Vessel (2007), 0 descendants of its own

Source page: https://510kreport.com/device/K011355
Methodology: https://510kreport.com/methodology