K-number	K141381
Device name	DURADIAGNOST
Applicant	Philips Healthcare (Suzhou) Co., Ltd.
Product code	KPR
Device class	Class II
Decision date	Jun 12, 2014
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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DURADIAGNOST

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