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

DEFINE System (AG612444A)

K Number: K242598 · Decision Nov 14, 2024
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
77
Applicant Total
15
Review Days
76

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Basic Information

Device Name
DEFINE System (AG612444A)
K Number
K242598
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
InMode , Ltd.
Date Received
August 30, 2024
Decision Date
November 14, 2024
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

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Other Clearances by InMode , Ltd.

K Number Device Name
K251254 Ignite RF System
K251632 Optimas MAX System
K240780 InMode RF System
K240017 InMode System with the Morpheus8 90 Applicator
K233642 InMode RF System
K231495 The Evolve System with the Transform Applicator
K231790 The InMode System with the Morpheus8 Applicators
K221571 InMode Multi-system
K210877 Evolve System with the T3 Applicator
K201285 InMode Evolve System with the Tone Applicator
Search all 15 clearances from InMode , Ltd. →