K-number	K011283
Device name	MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE
Applicant	The Kendall Company
Product code	NGT
Device class	Class II
Decision date	Oct 15, 2001
Decision	Substantially Equivalent
Regulation	880.5200

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View the full FDA submission: accessdata.fda.gov

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MONOJECT PREFILL 0.9% SODIUM CHLORIDE FLUSH SYRINGE

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