K-number	K091860
Device name	AESKULISA MPO, MODEL 30-7303US
Applicant	Aesku Diagnostics
Product code	MOB
Device class	Class II
Decision date	Feb 23, 2010
Decision	Substantially Equivalent
Regulation	866.5660

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View the full FDA submission: accessdata.fda.gov

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AESKULISA MPO, MODEL 30-7303US

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