Class Class II

MAGNETOM Vida (K213805)

K213805 2023-02-24 Traditional
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Description

MAGNETOM Vida by Siemens Medical Solutions USA, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK213805
Clearance Date2023-02-24
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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