FDA 510(k)

LED Phototherapy Device

K-Number: K162098 · 2017-01-30

ApplicantLi-Tek Electronic Technology Corporation

Decision Date2017-01-30

Product CodeOLP

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LED Phototherapy Device is a medical device manufactured by Li-Tek Electronic Technology Corporation. It received FDA 510(k) clearance on 2017-01-30 under approval number K162098. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED Phototherapy Device?

LED Phototherapy Device is a medical device that received FDA 510(k) clearance on 2017-01-30. It is manufactured by Li-Tek Electronic Technology Corporation. The 510(k) number is K162098.

When was LED Phototherapy Device approved by the FDA?

LED Phototherapy Device received FDA 510(k) clearance on 2017-01-30, under approval number K162098.

What company makes LED Phototherapy Device?

LED Phototherapy Device is manufactured by Li-Tek Electronic Technology Corporation.

What is the FDA product code for LED Phototherapy Device?

The FDA product code for LED Phototherapy Device is OLP.

Other Devices by Li-Tek Electronic Technology Corporation

K162652Smart Photon Micro-current Device, Model: EP-300 K162106Micro-current Wrinkle Reduction Facial service, model EP-400

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.