K-number	K970604
Device name	VIEWPOINT - 3.0 SOFTWARE
Applicant	Philips Medical Systems (Cleveland), Inc.
Product code	HAW
Device class	Class II
Decision date	May 19, 1997
Decision	Substantially Equivalent
Regulation	882.4560

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View the full FDA submission: accessdata.fda.gov

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VIEWPOINT - 3.0 SOFTWARE

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