K233664

IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY,UI06 IG,)

510(k) number: K233664
Device name: IPL Hair Removal Device (UI06 PN, UI06 PL, UI06 JL, UI06 BR, UI06 DB, UI06 PR, UI06 OG, UI06 RD,UI06 WH, UI06 MG, UI06 OB, UI06 LY,UI06 IG,)
Applicant: Shenzhen Ulike Smart Electronics Co., Ltd. CN
Product code: OHT — Light Based Over-The-Counter Hair Removal
Decision date: 2024-01-11
Date received: 2023-11-15
Decision: Substantially Equivalent
Clearance type: Traditional
Advisory committee: General, Plastic Surgery

This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.

Official FDA record: K233664

Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.