← Back to catalogue

IPL Hair Removal Device - KA-18

FDA 510(k)

Class II (US FDA 510(k))

510(k) K253304

by Dongguan Lide Electric Appliance Co., Ltd.

Identifiers

510(k) Number
K253304 FDA 510(k)
FDA Product Code
OHT FDA 510(k)
Models / Variants
KA-10 FDA 510(k)
KA-11 FDA 510(k)
KA-11C FDA 510(k)
KA-11D FDA 510(k)
KA-18 FDA 510(k)
KA-20 FDA 510(k)
KA-21 FDA 510(k)
KA-21C 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 Hair Removal Device - KA-18 by Dongguan Lide Electric Appliance Co., Ltd. — Class II — FDA_510K — listed in FDA 510(k) — 8 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Dongguan Lide Electric Appliance Co., Ltd.

Sources (1)

  • FDA 510(k) K253304 24 fields · synced Jun 19, 2026