Class Class II

Everion+ System (K213863)

K213863 2023-02-23 Traditional
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Description

Everion+ System by Biofourmis Singapore Pte., Ltd. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213863
Clearance Date2023-02-23
Clearance TypeTraditional
Product CodeMSX
Regulation Number870.2300

Categories

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