K-number	K024200
Device name	INNOVA 2000 AND INNOVA 2000S (MOBILE VERSION)
Applicant	Ge Medical Systems, Inc.
Product code	OWB
Device class	Class II
Decision date	Jan 16, 2003
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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INNOVA 2000 AND INNOVA 2000S (MOBILE VERSION)

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