Class Class II

ZEUS System (K222389)

K222389 2023-02-15 Traditional
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Description

ZEUS System by iRhythm Technologies, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK222389
Clearance Date2023-02-15
Clearance TypeTraditional
Product CodeDQK
Regulation Number870.1425

Categories

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