K-number	K162395
Device name	MP DOA-10 Panel Test Cup, MP DOA-11 Panel Test Cup
Applicant	Mp Biomedicals, LLC
Product code	DIO
Device class	Class II
Decision date	Jun 2, 2017
Decision	Substantially Equivalent
Regulation	862.3250

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Source

View the full FDA submission: accessdata.fda.gov

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MP DOA-10 Panel Test Cup, MP DOA-11 Panel Test Cup

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