K-number	K983069
Device name	PHILIPS DUO DIAGNOST
Applicant	Philips Medical Systems North America, Inc.
Product code	OWB
Device class	Class II
Decision date	Nov 2, 1998
Decision	Substantially Equivalent
Regulation	892.1650

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View the full FDA submission: accessdata.fda.gov

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PHILIPS DUO DIAGNOST

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