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FDA-clearance

July 22, 2021 cman FDA, Literature

510(k) Premarket Notification

Device Classification Namesystem, nuclear magnetic resonance imaging
510(k) NumberK210415
Device nameQSM software, QSMetric
ApplicantMedimagemetric LLC
171 Floral Ave
Johnson City,  NY  13790
Regulation Number892.1000
Decision Date07/22/2021

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