510(k) K220214

Device
Painless IPL System - KDT750
Applicant
Shanghai Omni Laser Skinology Co., Ltd.
510(k) number
K220214
Product code
ONF
Decision
Substantially Equivalent (SESE)
Decision date
2023-02-18
Date received
2022-01-26
Regulation
878.4810
Classification name
Powered Light Based Non-Laser Surgical Instrument With Thermal Effect
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N

Related Records

Applicant Contact

Contact
Avril Ouyang
Address
Floor 3, Bldg. 3, #227, Mingqiang Rd. Songjiang District Shanghai CN 201612 201612

FDA Registration Numbers

Source Documents

510(k) summary PDF

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