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FDA 510(k)

IPL Hair Removal Device

K-Number: K232939 · 2023-12-15

ApplicantShenzhen Borria Technology Co., Ltd.
Decision Date2023-12-15
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal Device is a medical device manufactured by Shenzhen Borria Technology Co., Ltd.. It received FDA 510(k) clearance on 2023-12-15 under approval number K232939. 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 2023-12-15. It is manufactured by Shenzhen Borria Technology Co., Ltd.. The 510(k) number is K232939.

When was IPL Hair Removal Device approved by the FDA?

IPL Hair Removal Device received FDA 510(k) clearance on 2023-12-15, under approval number K232939.

What company makes IPL Hair Removal Device?

IPL Hair Removal Device is manufactured by Shenzhen Borria Technology Co., Ltd..

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

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

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Other Devices by Shenzhen Borria Technology Co., Ltd.

K213020IPL hair removal machine K242385LED Therapy Mask (MN1, M226)

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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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