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Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 R…

FDA 510(k)

Class II (US FDA 510(k))

510(k) K250938

by Shenzhen Ulike Smart Electronics Co., Ltd.

Identifiers

510(k) Number
K250938 FDA 510(k)
FDA Product Code
OHT FDA 510(k)
Models / Variants
Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 RM, MI01 WG, MI01 WH, MI01 BK FDA 510(k)
UI04S PP, UI04S BU, UI04S WH, UI04S PN) FDA 510(k)

Classification

Device Class
Class II FDA 510(k)
Legislation / Framework
21 CFR Part 878.4810 FDA 510(k)
Regulation Number
878.4810 FDA 510(k)
Advisory Committee
General, Plastic Surgery FDA 510(k)
FDA Decision
SESE Substantially Equivalent FDA 510(k)

Ice Cooling IPL Hair Removal Device (MI01 LP, MI01 CB, MI01 GR, MI01 PP, MI01 R… by Shenzhen Ulike Smart Electronics Co., Ltd. — Class II — FDA_510K — listed…

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Shenzhen Ulike Smart Electronics Co., Ltd.

Sources (1)

  • FDA 510(k) K250938 24 fields · synced Jun 19, 2026