# K241120: Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S)

- Pathway: 510(k) (Traditional)
- Applicant: Qiaocheng LI (Dongguan) Medical Instruments Co., Ltd.
- Decided: Jun 24, 2024 after 62 days
- Product code: OHT (Light Based Over-The-Counter Hair Removal)
- 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
Longest line of descent: 24 generations back to K950019 (1995). 65 ancestors in all.
1 later device descends from it; 1 cites 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)
- K231613: Intense pulsed light device, Model (s): DE01A-B, DE01A-G, DE01B-B, DE01B-G, DE01C-B, DE01C-G, DE02A-B, DE02A-G, DE02B-B, DE02B-G, DE02C-B, DE02C-G., Zhuzhou Goldenhot Medical Technology Co., Ltd. (2023) Summary page 5.
- K221569: Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K, Shenzhen Fansizhe Science and Technology Co., Ltd. (2022) Summary page 5.

## Most influential descendants
- K252234: IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S) (2025), 0 descendants of its own

## Indications for use
Intense pulsed light therapy apparatus is an over-the-counter device intended for removal of unwanted body and/or facial hair.

Source page: https://510kreport.com/device/K241120
Methodology: https://510kreport.com/methodology