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FDA 510(k)

Home Use Hair Removal Device/T1, T2, T3

K-Number: K172883 · 2018-02-12

ApplicantShenzhen Mareal Tech Co., Ltd.
Decision Date2018-02-12
Product CodeOHT
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Home Use Hair Removal Device/T1, T2, T3 is a medical device manufactured by Shenzhen Mareal Tech Co., Ltd.. It received FDA 510(k) clearance on 2018-02-12 under approval number K172883. 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 Home Use Hair Removal Device/T1, T2, T3?

Home Use Hair Removal Device/T1, T2, T3 is a medical device that received FDA 510(k) clearance on 2018-02-12. It is manufactured by Shenzhen Mareal Tech Co., Ltd.. The 510(k) number is K172883.

When was Home Use Hair Removal Device/T1, T2, T3 approved by the FDA?

Home Use Hair Removal Device/T1, T2, T3 received FDA 510(k) clearance on 2018-02-12, under approval number K172883.

What company makes Home Use Hair Removal Device/T1, T2, T3?

Home Use Hair Removal Device/T1, T2, T3 is manufactured by Shenzhen Mareal Tech Co., Ltd..

What is the FDA product code for Home Use Hair Removal Device/T1, T2, T3?

The FDA product code for Home Use Hair Removal Device/T1, T2, T3 is OHT.

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Other Devices by Shenzhen Mareal Tech Co., Ltd.

K220248Home use hair removal device

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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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