510(k) K232192

Device
Venus Versa PRO System
Applicant
Venus Concept, Inc.
510(k) number
K232192
Product code
ONF
Decision
Substantially Equivalent (SESE)
Decision date
2023-09-11
Date received
2023-07-24
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
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
William H. McGrail
Address
1800 Bering Dr. San Jose CA US 95112 95112

FDA Registration Numbers

Source Documents

510(k) summary PDF

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