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FDA 510(k)

LED Lip Perfector, model: ZC-05

K-Number: K223642 · 2023-03-09

ApplicantLight Tree Ventures Europe B.V.
Decision Date2023-03-09
Product CodeILY
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

LED Lip Perfector, model: ZC-05 is the device name listed in this FDA 510(k) record. The listed applicant is Light Tree Ventures Europe B.V.. It received FDA 510(k) clearance on 2023-03-09 under 510(k) number K223642. The device is classified under product code ILY. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LED Lip Perfector, model: ZC-05?

LED Lip Perfector, model: ZC-05 is a medical device that received FDA 510(k) clearance on 2023-03-09. The listed applicant is Light Tree Ventures Europe B.V.. The 510(k) number is K223642.

When did LED Lip Perfector, model: ZC-05 receive FDA 510(k) clearance?

LED Lip Perfector, model: ZC-05 received FDA 510(k) clearance on 2023-03-09, under 510(k) number K223642.

Who is the listed applicant for LED Lip Perfector, model: ZC-05?

The FDA 510(k) record lists Light Tree Ventures Europe B.V. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LED Lip Perfector, model: ZC-05?

The FDA product code for LED Lip Perfector, model: ZC-05 is ILY.

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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.

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