510(k) K233123

Device
SILKRO
Applicant
Hironic Co., Ltd.
510(k) number
K233123
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2024-06-24
Date received
2023-09-27
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Gwijin Lee
Address
19f, U-Tower, 767, Sinsu-Ro Suji-Gu Yongin-Si KR 16827 16827

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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