Class Class II

MuscleView (K241331)

K241331 2024-10-01 Traditional
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Description

MuscleView by Springbok, Inc., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241331
Clearance Date2024-10-01
Clearance TypeTraditional
Product CodeLNH
Regulation Number892.1000

Categories

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