Class Class II

LOGIQ Fortis (K253366)

K253366 2026-01-07 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK253366
Clearance Date2026-01-07
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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