K233679

IPL Hair Removal Device (UI04 MK,UI04 BN,UI04 BU,UI04 CB,UI04 GY,UI04 LG,UI04 DG,UI04 PL,UI04 PN,UI04 SD,UI04 SG,UI04 MG)

510(k) number
K233679
Device name
IPL Hair Removal Device (UI04 MK,UI04 BN,UI04 BU,UI04 CB,UI04 GY,UI04 LG,UI04 DG,UI04 PL,UI04 PN,UI04 SD,UI04 SG,UI04 MG)
Applicant
Shenzhen Ulike Smart Electronics Co., Ltd. CN
Product code
OHT — Light Based Over-The-Counter Hair Removal
Decision date
2024-01-05
Date received
2023-11-16
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: K233679
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.