Class Class II

ViewMateTM Ultrasound System (K251820)

K251820 2025-09-12 Traditional
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Description

ViewMateTM Ultrasound System by Shenzhen Mindray Bio-Medical Electronics Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251820
Clearance Date2025-09-12
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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