K-number	K173433
Device name	ProxiDiagnost N90
Applicant	Philips Medical Systems Dmc GmbH
Product code	OWB
Device class	Class II
Decision date	Feb 5, 2018
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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ProxiDiagnost N90

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