K-number	K132082
Device name	AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECK
Applicant	Aesku Diagnostics
Product code	MST
Device class	Class II
Decision date	Dec 5, 2013
Decision	Substantially Equivalent
Regulation	866.5750

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View the full FDA submission: accessdata.fda.gov

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AESKULISA DGP-A, AESKULISA DGP-G,AESKULISA DGP-CHECK

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