K-number	K992051
Device name	RADIFOCUS OPTITORQUE
Applicant	Terumo Medical Corp.
Product code	DQO
Device class	Class II
Decision date	Aug 10, 1999
Decision	Substantially Equivalent
Regulation	870.1200

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Source

View the full FDA submission: accessdata.fda.gov

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RADIFOCUS OPTITORQUE

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