K-number	K921295
Device name	INTRAVENOUS CATHETERS MODIFICATIONS
Applicant	Critikon Company, LLC
Product code	FGO
Device class	Class II
Decision date	May 17, 1993
Decision	Substantially Equivalent
Regulation	876.4680

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View the full FDA submission: accessdata.fda.gov

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INTRAVENOUS CATHETERS MODIFICATIONS

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