Class Class II

Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) (K234009)

K234009 2024-07-12 Traditional
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Description

Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) by Mighty Oak Medical — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK234009
Clearance Date2024-07-12
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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