K-number	K151221
Device name	Kubtec DIGIVIEW 395
Applicant	Kub Technologies, Inc.
Product code	MQB
Device class	Class II
Decision date	Jun 23, 2015
Decision	Substantially Equivalent
Regulation	892.1680

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View the full FDA submission: accessdata.fda.gov

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Kubtec DIGIVIEW 395

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