Class Class II

AiMIFY (1.x) (K240290)

K240290 2024-08-21 Traditional
Home/ Devices/ AiMIFY (1.x) (K240290)

Description

AiMIFY (1.x) by Subtle Medical, Inc. — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK240290
Clearance Date2024-08-21
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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