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FDA 510(k)

IPL Home Use Hair Removal Device

K-Number: K211922 · 2021-09-20

ApplicantShenzhen Beauty Every Moment Intelligent Electric Co., Ltd.
Decision Date2021-09-20
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Home Use Hair Removal Device is a medical device manufactured by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.. It received FDA 510(k) clearance on 2021-09-20 under approval number K211922. 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 IPL Home Use Hair Removal Device?

IPL Home Use Hair Removal Device is a medical device that received FDA 510(k) clearance on 2021-09-20. It is manufactured by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.. The 510(k) number is K211922.

When was IPL Home Use Hair Removal Device approved by the FDA?

IPL Home Use Hair Removal Device received FDA 510(k) clearance on 2021-09-20, under approval number K211922.

What company makes IPL Home Use Hair Removal Device?

IPL Home Use Hair Removal Device is manufactured by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd..

What is the FDA product code for IPL Home Use Hair Removal Device?

The FDA product code for IPL Home Use Hair Removal Device is OHT.

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Other Devices by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

K211185IPL Home Use Hair Removal Device K221001IPL Home Use Hair Removal Device K240583IPL Home Use Hair Removal Device (D-1199, D-T099, D-T018, D-T019, D-T003B, D-T003W, D-T018Y, D-T019Y, D-1196B, D-1196W, D-1196C, D-1196C1, D-T099K, D-T099KW, D-T012, D-T012W)

Related Devices (Code: OHT)

K162231iPulse SmoothSkin Gold Hair Removal Device, Venus Silk.expertCyden Limited K161089sensiLight MiniEl Global Trade, Ltd. K160968iPulse SmoothSkin Gold Hair Removal DeviceCyden Limited K172181micro IPLEl Global Trade, Ltd. K171433Silk'n InfinityHome Skinovations , Ltd. K170269Hee HR MiniOriental Inspiration Limited

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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