K-number	K133524
Device name	PVMED DDR 2430T
Applicant	Portavision Medical, LLC
Product code	MQB
Device class	Class II
Decision date	Apr 16, 2014
Decision	Substantially Equivalent
Regulation	892.1680

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Source

View the full FDA submission: accessdata.fda.gov

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PVMED DDR 2430T

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