K-number	K203087
Device name	CombiDiagnost R90
Applicant	Philips Medical Systems Dmc GmbH
Product code	JAA
Device class	Class II
Decision date	Dec 3, 2020
Decision	Substantially Equivalent
Regulation	892.1650

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Source

View the full FDA submission: accessdata.fda.gov

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CombiDiagnost R90

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