K-number	K100420
Device name	PHILIPS OBTRACEVUE MODEL SW REV. G.00
Applicant	Philips Medizin Systeme Boeblingen GmbH
Product code	HGM
Device class	Class II
Decision date	Jul 26, 2010
Decision	Substantially Equivalent
Regulation	884.2740

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View the full FDA submission: accessdata.fda.gov

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PHILIPS OBTRACEVUE MODEL SW REV. G.00

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