K-number	K000310
Device name	VOYAGER 6.0 SOFTWARE OPTION
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	HAW
Device class	Class II
Decision date	Feb 15, 2000
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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VOYAGER 6.0 SOFTWARE OPTION

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