K-number	K852299
Device name	TERUMO SENSIBEAD EIA HGH KIT
Applicant	Terumo Medical Corp.
Product code	CFL
Device class	Class I
Decision date	Jul 9, 1985
Decision	Substantially Equivalent
Regulation	862.1370

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View the full FDA submission: accessdata.fda.gov

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TERUMO SENSIBEAD EIA HGH KIT

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