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FDA 510(k)

IPL Hair Removal

K-Number: K220927 · 2022-06-02

ApplicantShenzhen Qiaochengli Technology Co., Ltd.
Decision Date2022-06-02
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

IPL Hair Removal is a medical device manufactured by Shenzhen Qiaochengli Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-06-02 under approval number K220927. 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?

IPL Hair Removal is a medical device that received FDA 510(k) clearance on 2022-06-02. It is manufactured by Shenzhen Qiaochengli Technology Co., Ltd.. The 510(k) number is K220927.

When was IPL Hair Removal approved by the FDA?

IPL Hair Removal received FDA 510(k) clearance on 2022-06-02, under approval number K220927.

What company makes IPL Hair Removal?

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

What is the FDA product code for IPL Hair Removal?

The FDA product code for IPL Hair Removal is OHT.

Other Devices by Shenzhen Qiaochengli Technology Co., Ltd.

K211174IPL Hair Removal K252234IPL Home Use Hair Removal Device (Models: FDA11, FDA12, FDA13, FDA14, FDA15, FDA16, FDA17, FDA18, FDA19, FDA20, FDA21S, FDA22S, FDA23S, FDA24S, FDA25, FDA26, FDA27, FDA28, FDA29S, FDA30S, FDA31S)

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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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