Class Class II

HiTop® (Models: HiToP®4touch, HiToP®2touch, HiToP®1touch) (K213655)

K213655 2023-01-17 Traditional
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Description

HiTop® (Models: HiToP®4touch, HiToP®2touch, HiToP®1touch) by Hilltek, LLC — FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213655
Clearance Date2023-01-17
Clearance TypeTraditional
Product CodeIPF
Regulation Number890.5850

Categories

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