Class Class II

FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630) (K223902)

K223902 2023-03-02 Traditional
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Description

FibroScan® device (Models: 502 Touch, 530 Compact, 430 Mini+, 230, and 630) by Echosens — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223902
Clearance Date2023-03-02
Clearance TypeTraditional
Product CodeIYO
Regulation Number892.1560

Categories

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