Class Class II

Acorn 3D Software (AC-SEG-4009); Acorn 3DP Model (AC-101-XX) (K251532)

K251532 2025-11-03 Traditional
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Description

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

Regulatory Information

Device ClassClass Class II
510(k) NumberK251532
Clearance Date2025-11-03
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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