Class Class II

UltraSight Guidance (K251416)

K251416 2025-12-17 Traditional
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Description

UltraSight Guidance by Ultrasight , Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251416
Clearance Date2025-12-17
Clearance TypeTraditional
Product CodeQJU
Regulation Number892.2100

Categories

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