Light Based Hair Removal Device
K-Number: K232846 · 2023-12-07
Decision Date2023-12-07
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Light Based Hair Removal Device is a medical device manufactured by Shenzhen Meik Beauty Industry Co., Ltd.. It received FDA 510(k) clearance on 2023-12-07 under approval number K232846. The device is classified under product code OHT. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Light Based Hair Removal Device?
Light Based Hair Removal Device is a medical device that received FDA 510(k) clearance on 2023-12-07. It is manufactured by Shenzhen Meik Beauty Industry Co., Ltd.. The 510(k) number is K232846.
When was Light Based Hair Removal Device approved by the FDA?
Light Based Hair Removal Device received FDA 510(k) clearance on 2023-12-07, under approval number K232846.
What company makes Light Based Hair Removal Device?
Light Based Hair Removal Device is manufactured by Shenzhen Meik Beauty Industry Co., Ltd..
What is the FDA product code for Light Based Hair Removal Device?
The FDA product code for Light Based Hair Removal Device is OHT.
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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.