K-number	K840673
Device name	SENSIBEAD EIA DIGOXIN KIT
Applicant	Terumo Medical Corp.
Product code	KXT
Device class	Class II
Decision date	Mar 12, 1984
Decision	Substantially Equivalent
Regulation	862.3320

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View the full FDA submission: accessdata.fda.gov

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SENSIBEAD EIA DIGOXIN KIT

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