K-number	K122589
Device name	DFP4343C7
Applicant	Mdi Consultants, Inc.
Product code	KPR
Device class	Class II
Decision date	Oct 5, 2012
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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DFP4343C7

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