K-number	K140469
Device name	MR SYRINGE DUAL PACK
Applicant	Coeur, Inc.
Product code	DXT
Device class	Class II
Decision date	Jul 28, 2014
Decision	Substantially Equivalent
Regulation	870.1650

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View the full FDA submission: accessdata.fda.gov

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MR SYRINGE DUAL PACK

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