LED Phototherapy Device
K-Number: K162098 · 2017-01-30
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.