K-number	K011991
Device name	MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR
Applicant	Medrad, Inc.
Product code	DXT
Device class	Class II
Decision date	Aug 21, 2001
Decision	Substantially Equivalent
Regulation	870.1650

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO MEDRAD SPECTRIS MR INJECTOR

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