K-number	K891769
Device name	MAGNISCAN 5000 MR SYSTEM
Applicant	General Electric Co.
Product code	LNH
Device class	Class II
Decision date	Jun 15, 1989
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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MAGNISCAN 5000 MR SYSTEM

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