Class Class II

LOGIQ E10s (K251963)

K251963 2025-10-29 Traditional
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Description

LOGIQ E10s by GE Medical Systems Ultrasound and Primary Care Diagnostics, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251963
Clearance Date2025-10-29
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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