Class Class II

Neuro20 Pro System (K223797)

K223797 2023-02-23 Traditional
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Description

Neuro20 Pro System by Neuro20 Technologies — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223797
Clearance Date2023-02-23
Clearance TypeTraditional
Product CodeNGX
Regulation Number890.5850

Categories

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