LED Eye Perfector, model: EY-36A, EY-36B
K-Number: K221444 · 2022-12-08
ApplicantLight Tree Ventures Europe B.V.
Decision Date2022-12-08
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
LED Eye Perfector, model: EY-36A, EY-36B is a medical device manufactured by Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2022-12-08 under approval number K221444. 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 Eye Perfector, model: EY-36A, EY-36B?
LED Eye Perfector, model: EY-36A, EY-36B is a medical device that received FDA 510(k) clearance on 2022-12-08. It is manufactured by Light Tree Ventures Europe B.V.. The 510(k) number is K221444.
When was LED Eye Perfector, model: EY-36A, EY-36B approved by the FDA?
LED Eye Perfector, model: EY-36A, EY-36B received FDA 510(k) clearance on 2022-12-08, under approval number K221444.
What company makes LED Eye Perfector, model: EY-36A, EY-36B?
LED Eye Perfector, model: EY-36A, EY-36B is manufactured by Light Tree Ventures Europe B.V..
What is the FDA product code for LED Eye Perfector, model: EY-36A, EY-36B?
The FDA product code for LED Eye Perfector, model: EY-36A, EY-36B 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.