K-number	K103290
Device name	EDLEN IMAGING - GEMINI DUSB
Applicant	Edlen Imaging, LLC
Product code	MUH
Device class	Class II
Decision date	Sep 19, 2011
Decision	Substantially Equivalent
Regulation	872.1800

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View the full FDA submission: accessdata.fda.gov

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EDLEN IMAGING - GEMINI DUSB

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