K-number	K071219
Device name	ATHENA MULTI-LYTE GBM TEST SYSTEM
Applicant	Zeus Scientific, Inc.
Product code	MVJ
Device class	Class II
Decision date	Dec 6, 2007
Decision	Substantially Equivalent
Regulation	866.5660

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View the full FDA submission: accessdata.fda.gov

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ATHENA MULTI-LYTE GBM TEST SYSTEM

Everything you need for a 510(k) submission. Nothing you don't.