Class Class II

ViVY (K250376)

K250376 2025-11-05 Traditional
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Description

ViVY by Viatherm Therapeutics, LLC, an FDA 510(k) cleared physical medicine device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250376
Clearance Date2025-11-05
Clearance TypeTraditional
Product CodeIMJ
Regulation Number890.5290

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