Q-Rejuvalight Pro Facewear (Model: P19-0023)
K-Number: K230042 · 2023-04-28
ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-04-28
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Q-Rejuvalight Pro Facewear (Model: P19-0023) is a medical device manufactured by Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-04-28 under approval number K230042. 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 Q-Rejuvalight Pro Facewear (Model: P19-0023)?
Q-Rejuvalight Pro Facewear (Model: P19-0023) is a medical device that received FDA 510(k) clearance on 2023-04-28. It is manufactured by Light Tree Ventures Europe B.V.. The 510(k) number is K230042.
When was Q-Rejuvalight Pro Facewear (Model: P19-0023) approved by the FDA?
Q-Rejuvalight Pro Facewear (Model: P19-0023) received FDA 510(k) clearance on 2023-04-28, under approval number K230042.
What company makes Q-Rejuvalight Pro Facewear (Model: P19-0023)?
Q-Rejuvalight Pro Facewear (Model: P19-0023) is manufactured by Light Tree Ventures Europe B.V..
What is the FDA product code for Q-Rejuvalight Pro Facewear (Model: P19-0023)?
The FDA product code for Q-Rejuvalight Pro Facewear (Model: P19-0023) 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.