K-number	K090811
Device name	INSPIRA HD, MODEL: NL1000
Applicant	Neurologica Corporation
Product code	KPS
Device class	Class II
Decision date	Aug 27, 2009
Decision	Substantially Equivalent
Regulation	892.1200

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View the full FDA submission: accessdata.fda.gov

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INSPIRA HD, MODEL: NL1000

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