K-number	K112057
Device name	KDL SYRINGES AND NEEDLE
Applicant	Shanghai Kindly Enterprise Dev. Group Co.,
Product code	FMF
Device class	Class II
Decision date	Dec 14, 2011
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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KDL SYRINGES AND NEEDLE

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