K-number	K193644
Device name	E-COM DR-2000 DR
Applicant	Livermoretech, Inc.
Product code	MQB
Device class	Class II
Decision date	Feb 14, 2020
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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E-COM DR-2000 DR

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