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510(k) K230593

Device
Victan
Applicant
Jiangsu Haize Medical Scientific Development Co., Ltd.
510(k) number
K230593
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2023-05-30
Date received
2023-03-03
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
Vincy Gao
Address
#99, Furongzhongsan Rd., Xishan Economical Development Zone Wuxi CN 214000 214000

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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