# K131859: Multifunctional Series

- Pathway: 510(k) (Traditional)
- Applicant: Beijing Honkon Technologies Co., Ltd.
- Decided: Oct 18, 2013 after 116 days
- Product code: ONF (Powered Light Based Non-Laser Surgical Instrument With Thermal Effect)
- 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: 12 generations back to K910422 (1992). 91 ancestors in all.
3 later devices descend from it; 1 cites it directly.
0 of 95 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122995: Intense Pulsed Light (Ipl) Systems, Beijing Kes Biology Technology Co., Ltd. (2013) Summary page 2.
- K093627: Ipulselight Ipl System, Models HS 300C and HS 650, Shanghai Apolo Medical Technologies Co., Ltd. (2011) Summary page 2.

## Most influential descendants
- K140668: Platinumgmt Ipl System Cloud (2014), 2 descendants of its own
- K153717: Venus Versa System (2016), 1 descendant of its own
- K232192: Venus Versa PRO System (2023), 0 descendants of its own

## Indications for use
The Multifunctional Series device (inclusive of the handpiece used to deliver pulsed-light energy) are indicated for use in surgical, aesthetic and cosmetic applications in hair removal, moderate inflammatory acne, and benign cutaneous vascular lesions.

Source page: https://510kreport.com/device/K131859
Methodology: https://510kreport.com/methodology