FDA 510(k), K041112, MAGNETOM ESPREE SYSTEM

FDA 510(k), K041112, MAGNETOM ESPREE SYSTEM

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510(K) Number: K041112
Device Name: MAGNETOM ESPREE SYSTEM
Manufacturer: SIEMENS MEDICAL SOLUTIONS USA, INC.
Device Classification Name: system, nuclear magnetic resonance imaging
Regulation Number: 892.1000
Classification Product Code: LNH
Date Received: 04/28/2004
Decision Date: 07/21/2004
Regulation Medical Specialty: Radiology

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