K-number	K082167
Device name	PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX
Applicant	Digimed Corporation
Product code	EHD
Device class	Class II
Decision date	Sep 26, 2008
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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PORTABLE X-RAY SYSTEM, MODELS DIOX-602, PROX

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