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IPL Hair Removal Device - KCA507

FDA 510(k)

Class II (US FDA 510(k))

510(k) K240282

by Dongguan Boyuan Intelligent Technology Co., Ltd

Identifiers

510(k) Number
K240282 FDA 510(k)
FDA Product Code
OHT FDA 510(k)
Models / Variants
model: KCA450 FDA 510(k)
KCA446 FDA 510(k)
KCA504 FDA 510(k)
KCA505 FDA 510(k)
KCA506 FDA 510(k)
KCA507 FDA 510(k)
KCA508 FDA 510(k)
KCA509 FDA 510(k)
KCA501 FDA 510(k)
KCA423 FDA 510(k)
KCA448 FDA 510(k)
KCA449 FDA 510(k)
KCA502 FDA 510(k)
KCA521 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 - KCA507 by Dongguan Boyuan Intelligent Technology Co., Ltd — Class II — FDA_510K — listed in FDA 510(k) — 14 models

Authorization Coverage (1 country)

Regulatory Authorizations

United States Active

FDA_510K

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Manufacturer

Manufacturer
Dongguan Boyuan Intelligent Technology Co., Ltd
FDA Applicant
Dongguan Boyuan Intelligent Technology Co.,Ltd

Sources (1)

  • FDA 510(k) K240282 24 fields · synced Jun 18, 2026