Class Class II

Auto Segmentation (K230082)

K230082 2023-05-04 Traditional
Home/ Devices/ Auto Segmentation (K230082)

Description

Auto Segmentation by Ge Medical Systems, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230082
Clearance Date2023-05-04
Clearance TypeTraditional
Product CodeQKB
Regulation Number892.2050

Categories

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