K-number	K982834
Device name	RESTGRID PACKAGE/GYROSCAN NT
Applicant	Philips Medical Systems North America, Inc.
Product code	LNH
Device class	Class II
Decision date	Oct 29, 1998
Decision	Substantially Equivalent
Regulation	892.1000

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View the full FDA submission: accessdata.fda.gov

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RESTGRID PACKAGE/GYROSCAN NT

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