K-number	K111103
Device name	DIGITAL X-RAY IMAGING SYSTEM
Applicant	Rf Co., Ltd.
Product code	MUH
Device class	Class II
Decision date	Jan 5, 2012
Decision	Substantially Equivalent
Regulation	872.1800

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Source

View the full FDA submission: accessdata.fda.gov

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DIGITAL X-RAY IMAGING SYSTEM

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