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FDA 510(k)

Hand-held IPL device (JOVS Hair Removal Device)

K-Number: K220645 · 2022-04-27

ApplicantShenzhen Qianyu Technology Co., Ltd.
Decision Date2022-04-27
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Hand-held IPL device (JOVS Hair Removal Device) is a medical device manufactured by Shenzhen Qianyu Technology Co., Ltd.. It received FDA 510(k) clearance on 2022-04-27 under approval number K220645. 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 Hand-held IPL device (JOVS Hair Removal Device)?

Hand-held IPL device (JOVS Hair Removal Device) is a medical device that received FDA 510(k) clearance on 2022-04-27. It is manufactured by Shenzhen Qianyu Technology Co., Ltd.. The 510(k) number is K220645.

When was Hand-held IPL device (JOVS Hair Removal Device) approved by the FDA?

Hand-held IPL device (JOVS Hair Removal Device) received FDA 510(k) clearance on 2022-04-27, under approval number K220645.

What company makes Hand-held IPL device (JOVS Hair Removal Device)?

Hand-held IPL device (JOVS Hair Removal Device) is manufactured by Shenzhen Qianyu Technology Co., Ltd..

What is the FDA product code for Hand-held IPL device (JOVS Hair Removal Device)?

The FDA product code for Hand-held IPL device (JOVS Hair Removal Device) is OHT.

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Other Devices by Shenzhen Qianyu Technology Co., Ltd.

K214113Hand-held IPL device(JOVS Graphene Hair Removal Device) K231800IPL Hair Removal Device, Model(s): JP1, JR3, JR8, JR9 K240360Wrinkle Treatment Device (JM2) K250227JOVS Electric Stimulation Beauty Device (JE2) K244020Wrinkle Treatment Device (JM1, JM2B)

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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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