K-number	K202564
Device name	DigitalDiagnost C90
Applicant	Philips Medical Systems Dmc GmbH
Product code	MQB
Device class	Class II
Decision date	Sep 30, 2020
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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DigitalDiagnost C90

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