Home Use Hair Removal Device/T1, T2, T3— 510(k) K172883

Substantially Equivalent

Shenzhen Mareal Tech Co., Ltd.

FDA 510(k) clearance K172883 for Home Use Hair Removal Device/T1, T2, T3, Substantially Equivalent on 2018-02-12. Applicant: Shenzhen Mareal Tech Co., Ltd..

Clearance details

Applicant: Shenzhen Mareal Tech Co., Ltd.
Product code: Code OHT
Advisory panel: General, Plastic Surgery
Date received: 2017-09-21
Decision date: 2018-02-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Shenzhen, CN

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