Class Class II

Planmed XFI (K250318)

K250318 2025-09-26 Traditional
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Description

Planmed XFI by Planmed OY, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250318
Clearance Date2025-09-26
Clearance TypeTraditional
Product CodeSFV
Regulation Number892.1750

Categories

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