Li-Tek Electronic Technology Corporation is one of 2135 FDA 510(k) medical device manufacturers from China in the dataset, ranked by real submission volume.
Li-Tek Electronic Technology Corporation - FDA 510(k) Cleared Devices
Recent clearances: Smart Photon Micro-current Device, Model: EP-300, Micro-current Wrinkle Reduction Facial service, model EP-400, LED Phototherapy Device
3
Total
3
Cleared
0
Denied
Li-Tek Electronic Technology Corporation has 3 FDA 510(k) cleared medical devices. Based in Dongguan, CN.
Historical record: 3 cleared submissions from 2017 to 2017. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Li-Tek Electronic Technology Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Guangzhou Leta Testing Technology Co., Ltd. as regulatory consultant.
FDA 510(k) Regulatory Record - Li-Tek Electronic Technology Corporation
3 devices