K-number	K011348
Device name	PHASE II GBM IGG ANTIBODY EIA TEST
Applicant	Scimedx Corp.
Product code	MVJ
Device class	Class II
Decision date	Jun 25, 2001
Decision	Substantially Equivalent
Regulation	866.5660

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View the full FDA submission: accessdata.fda.gov

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PHASE II GBM IGG ANTIBODY EIA TEST

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