Class Class II

neo315 (K231133)

K231133 2024-07-22 Traditional
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Description

neo315 by Neoscan Solution GmbH — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK231133
Clearance Date2024-07-22
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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