K-number	K001616
Device name	MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE
Applicant	Abbott Laboratories
Product code	FOZ
Device class	Class II
Decision date	Jul 27, 2000
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO SYRINGE PREFILLED WITH 0.9% SODIUM CHLORIDE

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