Class Class II

LOGIQ Totus (K253370)

K253370 2026-01-08 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK253370
Clearance Date2026-01-08
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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