FDA 510(k), K050456, MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM

FDA 510(k), K050456, MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM

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510(K) Number: K050456
Device Name: MEDRAD AVANTA FLUID MANAGEMENT INJECTION SYSTEM
Manufacturer: MEDRAD, INC.
Device Classification Name: injector and syringe, angiographic
Regulation Number: 870.1650
Classification Product Code: DXT
Date Received: 02/23/2005
Decision Date: 06/17/2005
Regulation Medical Specialty: Cardiovascular

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