K-number	K971924
Device name	BLUNT SYRINGE CANNULA
Applicant	B.Braun Medical, Inc.
Product code	FMI
Device class	Class II
Decision date	Sep 25, 1998
Decision	Substantially Equivalent
Regulation	880.5570

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View the full FDA submission: accessdata.fda.gov

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BLUNT SYRINGE CANNULA

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