Class Class II

InMode RF System (K240780)

K240780 2024-07-24 Traditional
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Description

InMode RF System by Inmode , Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240780
Clearance Date2024-07-24
Clearance TypeTraditional
Product CodeGEI
Regulation Number878.4400

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