510(k) K222958

Device
mJOULE RF System and Accessories
Applicant
Sciton, Inc
510(k) number
K222958
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2024-04-23
Date received
2022-09-27
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
Jay Patel
Address
925 Commercial St. Palo Alto CA US 94303 94303

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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