# K240583: IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)

- Pathway: 510(k) (Traditional)
- Applicant: Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.
- Decided: Jun 18, 2024 after 109 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: 21 generations back to K950019 (1995). 59 ancestors in all.
No later device cites it as a predicate yet.
0 of 60 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K211185: IPL Home Use Hair Removal Device, Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. (2021) Summary page 6.

## Indications for use
IPL Home Use Hair Removal Device is an over-the-counter device intended for removal of unwanted body and/or facial hair.

Source page: https://510kreport.com/device/K240583
Methodology: https://510kreport.com/methodology