# Shenzhen Jingkehui Electronic Co.., Ltd.

- Location (FDA's records): Mountain View, CA
- FDA decisions: 3 (2013–2015): 3 510(k) clearances
- Product codes: NUH (3)
- Predicates its devices cite: 3 (1 its own); citations of its devices by later devices: 4 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Prospera Corporation: 1 (https://510kreport.com/company/prospera)
- Iq Technologies, Inc.: 1 (https://510kreport.com/company/iq-technologies)

## Firms that cite its devices most
- Shenzhen Eapply Technology Co., Ltd.: 1 (https://510kreport.com/company/shenzhen-eapply-technology)
- Jkh USA, LLC: 1 (https://510kreport.com/company/jkh-usa)
- Jkh Health Co., Ltd.: 1 (https://510kreport.com/company/jkh-health)

## Its most-cited devices
- K141260: Electronic Pulse Stimulator (2014), cited by 3
- K131921: Electronic Pulse Stimulator (2013), cited by 1

## Recent decisions
- K150995: Electronic Pulse Stimulator (Jul 6, 2015)
- K141260: Electronic Pulse Stimulator (Sep 17, 2014)
- K131921: Electronic Pulse Stimulator (Nov 15, 2013)

Source page: https://510kreport.com/company/shenzhen-jingkehui-electronic