510(k) K231790

Device
The InMode System with the Morpheus8 Applicators
Applicant
InMode , Ltd.
510(k) number
K231790
Product code
GEI
Decision
Substantially Equivalent (SESE)
Decision date
2023-07-20
Date received
2023-06-20
Regulation
878.4400
Classification name
Electrosurgical, Cutting & Coagulation & Accessories
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Suhair Francis
Address
Tabor Bldg., Shaar Yokneam Pob 44 Yokneam Illit IL 2069200 2069200

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

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