K-number	K953495
Device name	EIA KIT FOR THE DETECTION OF GBM ANTIBODIES
Applicant	Scimedx Corp.
Product code	DBL
Device class	Class II
Decision date	Apr 10, 1996
Decision	Substantially Equivalent
Regulation	866.5660

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Source

View the full FDA submission: accessdata.fda.gov

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EIA KIT FOR THE DETECTION OF GBM ANTIBODIES

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