FDA 510(k), K042784, MEDRAD SPECTRIS SOLARIS EP MR INJECTOR SYSTEM

FDA 510(k), K042784, MEDRAD SPECTRIS SOLARIS EP MR INJECTOR SYSTEM

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510(K) Number: K042784
Device Name: MEDRAD SPECTRIS SOLARIS EP MR INJECTOR SYSTEM
Manufacturer:
Device Classification Name: Injector And Syringe, Angiographic
Regulation Number: 870.1650
Classification Product Code: DXT
Date Received: 10/06/2004
Decision Date: 12/10/2004
Regulation Medical Specialty: Cardiovascular
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