Class Class II

VX1+ (K223516)

K223516 2023-01-21 Traditional
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Description

VX1+ by Volta Medical — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223516
Clearance Date2023-01-21
Clearance TypeTraditional
Product CodeDQK
Regulation Number870.1425

Categories

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