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FDA 510(k)

LED Phototherapy Device

K-Number: K162098 · 2017-01-30

Decision Date2017-01-30
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LED Phototherapy Device is the device name listed in this FDA 510(k) record. The listed applicant is Li-Tek Electronic Technology Corporation. It received FDA 510(k) clearance on 2017-01-30 under 510(k) 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. The listed applicant is Li-Tek Electronic Technology Corporation. The 510(k) number is K162098.

When did LED Phototherapy Device receive FDA 510(k) clearance?

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

Who is the listed applicant for LED Phototherapy Device?

The FDA 510(k) record lists Li-Tek Electronic Technology Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LED Phototherapy Device?

The FDA product code for LED Phototherapy Device is OLP.

Other records listing Li-Tek Electronic Technology Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: OLP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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