K-number	K122416
Device name	ARTIGLASS L. O.R. GLASS SYRINGE
Applicant	Artiglass Srl
Product code	FMF
Device class	Class II
Decision date	May 3, 2013
Decision	Substantially Equivalent
Regulation	880.5860

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View the full FDA submission: accessdata.fda.gov

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ARTIGLASS L. O.R. GLASS SYRINGE

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