K-number	K896813
Device name	MODIFIED INTRAVENOUS CATHETER
Applicant	Safeguard Needle Co.
Product code	FOZ
Device class	Class II
Decision date	Oct 19, 1990
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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MODIFIED INTRAVENOUS CATHETER

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