LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)
K-Number: K241857 · 2024-10-11
Decision Date2024-10-11
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) is a medical device manufactured by Dongguan Boyuan Intelligent Technology Co.,Ltd. It received FDA 510(k) clearance on 2024-10-11 under approval number K241857. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)?
LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) is a medical device that received FDA 510(k) clearance on 2024-10-11. It is manufactured by Dongguan Boyuan Intelligent Technology Co.,Ltd. The 510(k) number is K241857.
When was LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) approved by the FDA?
LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) received FDA 510(k) clearance on 2024-10-11, under approval number K241857.
What company makes LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)?
LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) is manufactured by Dongguan Boyuan Intelligent Technology Co.,Ltd.
What is the FDA product code for LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293)?
The FDA product code for LED Light Therapy Device (KFB290, KFB291, KFB265, KFB293) is OHS.
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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.