K-number	K971181
Device name	THE MIDVIEW-MEDCON'S DICOM VIEWER
Applicant	Medcon , Ltd.
Product code	IZI
Device class	Class II
Decision date	Jul 29, 1997
Decision	Substantially Equivalent
Regulation	892.1600

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View the full FDA submission: accessdata.fda.gov

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THE MIDVIEW-MEDCON'S DICOM VIEWER

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