Class Class II

MIM – LesionID Pro (K251883)

K251883 2025-12-11 Traditional
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Description

MIM – LesionID Pro by Mim Software, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251883
Clearance Date2025-12-11
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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