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FDA 510(k)

IPL Hair Removal Device

K-Number: K183217 · 2019-02-15

Decision Date2019-02-15
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device is a medical device manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. It received FDA 510(k) clearance on 2019-02-15 under approval number K183217. 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 Hair Removal Device?

IPL Hair Removal Device is a medical device that received FDA 510(k) clearance on 2019-02-15. It is manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.. The 510(k) number is K183217.

When was IPL Hair Removal Device approved by the FDA?

IPL Hair Removal Device received FDA 510(k) clearance on 2019-02-15, under approval number K183217.

What company makes IPL Hair Removal Device?

IPL Hair Removal Device is manufactured by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd..

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

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

Related Clinical Trials

Other Devices by Touchbeauty Beauty & Health (Shenzhen) Co., Ltd.

Related Devices (Code: OHT)

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.