Class Class II

RMF-2000 (K220073)

K220073 2023-01-26 Traditional
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Description

RMF-2000 by DRTECH Corporation — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK220073
Clearance Date2023-01-26
Clearance TypeTraditional
Product CodeMUE
Regulation Number892.1715

Categories

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