FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

InMode System MiniFX Handpiece

K Number: K160329 · Decision Aug 19, 2016
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
21
Review Days
196

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Basic Information

Device Name
InMode System MiniFX Handpiece
K Number
K160329
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
Inmode MD , Ltd.
Date Received
February 5, 2016
Decision Date
August 19, 2016
Product Code
PBX
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
PBX Massager, Vacuum, Radio Frequency Induced Heat

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PBX), ordered by most recent decision date.

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Other Clearances by Inmode MD , Ltd.

K Number Device Name
K210492 InMode RF Pro System
K192695 InMode System with the Morpheus8 (Fractora) Applicators
K191855 EmFace Device
K183450 EmBody System
K182325 InMode RF System
K180719 InMode Diolaze System
K180189 InMode System with Fractora3D/3D-90 Applicators
K173677 InMode VLaze
K172302 InMode PLUS System
K171593 InMode RF System
Search all 21 clearances from Inmode MD , Ltd. →