K-number	K092830
Device name	DIGITAL X-RAY IMAGING SYSTEM, MODEL DRC-1000
Applicant	VATECH Co., Ltd.
Product code	KPR
Device class	Class II
Decision date	Jul 21, 2010
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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DIGITAL X-RAY IMAGING SYSTEM, MODEL DRC-1000

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