# K221569: Intense Pulsed Light (IPL) System, model: T013C, T015C, T015K

- Pathway: 510(k) (Special)
- Applicant: Shenzhen Fansizhe Science and Technology Co., Ltd.
- Decided: Jun 30, 2022 after 30 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: 1 generation back to K212881 (2022). 1 ancestor in all.
4 later devices descend from it; 3 cite it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K212881: Intense Pulsed Light (IPL) System, Shenzhen Fansizhe Science and Technology Co., Ltd. (2022) Summary page 5.

## Most influential descendants
- K251173: Intense Pulsed Light (IPL) System (T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T002AQ, T002AD, T002AF, T002BQ, T002BD, T002BF, T050KQ, T050KD, T050KF) (2025), 1 descendant of its own
- K241120: Intense pulsed light therapy apparatus (FDA01, FDA02, FDA03, FDA04S, FDA05S, FDA06, FDA06S, FDA07, FDA07S, FDA08, FDA09S, FDA10S) (2024), 1 descendant of its own
- K253881: Intense Pulsed Light (IPL) System (Models: T033KQ, T033KD, T033KF, T033MQ, T033MD, T033MF, T055KQ, T055KD, T055KH, T505KQ, T505KH, T505KF, SL-B505WM) (2025), 0 descendants of its own
- 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
The Intense Pulsed Light (IPL) System is an over-the-counter device intended for the removal of unwanted body hair.

Source page: https://510kreport.com/device/K221569
Methodology: https://510kreport.com/methodology