Class Class II

ProKnow DS (K251363)

K251363 2025-10-08 Traditional
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Description

ProKnow DS by Elekta Solutions AB, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251363
Clearance Date2025-10-08
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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