K-number	K991758
Device name	MONOJECT INSULIN SYRINGE
Applicant	The Kendal Co.
Product code	FMF
Device class	Class II
Decision date	Jun 14, 1999
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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MONOJECT INSULIN SYRINGE

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