K-number	K894230
Device name	PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735)
Applicant	Siemens Medical Laboratories, Inc.
Product code	IYE
Device class	Class II
Decision date	Aug 28, 1989
Decision	Substantially Equivalent
Regulation	892.5050

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View the full FDA submission: accessdata.fda.gov

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PATIENT DATA MANAGEMENT SYSTEM (PROJECT 735)

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