K-number	K945642
Device name	AGEN DIMERTEST GOLD EIA
Applicant	Agen Biomedical , Ltd.
Product code	GHH
Device class	Class II
Decision date	Oct 25, 1995
Decision	Substantially Equivalent
Regulation	864.7320

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View the full FDA submission: accessdata.fda.gov

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AGEN DIMERTEST GOLD EIA

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