Class Class II

CardIQ Suite (K233731)

K233731 2024-08-01 Traditional
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Description

CardIQ Suite by GE Medical Systems SCS — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK233731
Clearance Date2024-08-01
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750

Categories

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