FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

mJOULE RF System and Accessories

K Number: K222958 · Decision Apr 23, 2024
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
23
Review Days
574

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Basic Information

Device Name
mJOULE RF System and Accessories
K Number
K222958
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sciton, Inc
Date Received
September 27, 2022
Decision Date
April 23, 2024
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

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Other Clearances by Sciton, Inc

K Number Device Name
K251077 JOULE 1064nm System and Accessories
K213761 Joule diVa System
K213350 mJOULE System and Accessories
K182173 Joule System
K180508 JOULE SYSTEM
K173285 JOULE SYSTEM
K122567 JOULE 810/940/980 MULTI-PLATFORM SYSTEM
K111483 JOULE CLEARSENSE LASER SYSTEM
K101916 JOULE MULTI-PLATFORM SYSTEM
K081352 PROFILE MULTI-PLATFORM SYSTEM
Search all 23 clearances from Sciton, Inc →