Class Class II

Gnesis EMS Plus (K230261)

K230261 2023-06-06 Traditional
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Description

Gnesis EMS Plus by Creative Fitness Developments S.L. — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230261
Clearance Date2023-06-06
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850

Categories

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