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Recognized a 510(k)/PMA number — showing its clearance record and devices.

Clearance record K210877

Evolve System with the T3 Applicator · InMode , Ltd. · decided 2021-07-19 (SESE)

FDA 510(k) database ↗Summary PDF ↗

Devices

BrandModelCompanyProduct codesPrimary DI
Evolve SystemAG608081AINMODE M.D LTDGEI GZJ IPF PBX07290016633498