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IPL Home Use Hair Removal Device - D-T018Y

FDA 510(k)

Class II (US FDA 510(k))

510(k) K240583

by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

Identifiers

510(k) Number
K240583 FDA 510(k)
FDA Product Code
OHT FDA 510(k)
Models / Variants
D-1199 FDA 510(k)
D-T099 FDA 510(k)
D-T018 FDA 510(k)
D-T019 FDA 510(k)
D-T003B FDA 510(k)
D-T003W FDA 510(k)
D-T018Y FDA 510(k)
D-T019Y FDA 510(k)
D-1196B FDA 510(k)
D-1196W FDA 510(k)
D-1196C FDA 510(k)
D-1196C1 FDA 510(k)
D-T099K FDA 510(k)
D-T099KW FDA 510(k)
D-T012 FDA 510(k)
D-T012W 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)

IPL Home Use Hair Removal Device - D-T018Y by Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 16…

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Shenzhen Beauty Every Moment Intelligent Electric Co., Ltd.

Sources (1)

  • FDA 510(k) K240583 24 fields · synced Jun 18, 2026