K-number	K193101
Device name	Omnifix Low Dead Space Luer Lock Syringe
Applicant	B.Braun Medical, Inc.
Product code	FMF
Device class	Class II
Decision date	Mar 5, 2020
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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Omnifix Low Dead Space Luer Lock Syringe

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