K-number	K890092
Device name	HI STANDARD MAGNETIC RESONANCE DIAGNOSTIC DEVICE
Applicant	Health Images, Inc.
Product code	LNH
Device class	Class II
Decision date	Jun 23, 1989
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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HI STANDARD MAGNETIC RESONANCE DIAGNOSTIC DEVICE

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