Class Class II

Spectral Bone Marrow (K223514)

K223514 2023-03-09 Traditional
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Description

Spectral Bone Marrow by Ge Medical Systems, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223514
Clearance Date2023-03-09
Clearance TypeTraditional
Product CodeJAK
Regulation Number892.1750

Categories

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