K-number	K201234
Device name	BD SoloShot Mini Syringe/ BD Auto Disable Syringe
Applicant	Becton, Dickinson and Company
Product code	FMF
Device class	Class II
Decision date	Jul 15, 2020
Decision	Substantially Equivalent
Regulation	880.5860

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Source

View the full FDA submission: accessdata.fda.gov

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BD SoloShot Mini Syringe/ BD Auto Disable Syringe

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