K-number	K890330
Device name	MEDILOG 6000-FD REPORT GENERATOR
Applicant	Oxford Medilog, Inc.
Product code	DSI
Device class	Class II
Decision date	Apr 20, 1989
Decision	Substantially Equivalent
Regulation	870.1025

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View the full FDA submission: accessdata.fda.gov

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MEDILOG 6000-FD REPORT GENERATOR

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