Class Class II

Navigator (FMNVG15); Navigator XL (FMNVX06) (K240105)

K240105 2024-08-29 Traditional
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Description

Navigator (FMNVG15); Navigator XL (FMNVX06) by Forcemech International, LLC — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240105
Clearance Date2024-08-29
Clearance TypeTraditional
Product CodeITI
Regulation Number890.3860

Categories

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