K-number	K053175
Device name	AMEDITECH DRUGSMARTCUP
Applicant	Ameditech, Inc.
Product code	DKZ
Device class	Class II
Decision date	Dec 8, 2005
Decision	Substantially Equivalent
Regulation	862.3100

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View the full FDA submission: accessdata.fda.gov

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AMEDITECH DRUGSMARTCUP

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