K-number	K120889
Device name	AESKUSLIDES ANA HEP-2
Applicant	Aesku Diagnostics
Product code	DHN
Device class	Class II
Decision date	Oct 15, 2012
Decision	Substantially Equivalent
Regulation	866.5100

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Source

View the full FDA submission: accessdata.fda.gov

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AESKUSLIDES ANA HEP-2

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