K-number	K212493
Device name	KODEX EPD System 1.5.0
Applicant	Philips Medical Systems Nederland, B.V. (Pmsn)
Product code	DQK
Device class	Class II
Decision date	Oct 24, 2022
Decision	Substantially Equivalent
Regulation	870.1425

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View the full FDA submission: accessdata.fda.gov

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KODEX  EPD System 1.5.0

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KODEX EPD System 1.5.0