K-number	K931743
Device name	BURRON CARDIOVASCULAR ANGESTAT(TM)
Applicant	B.Braun Medical, Inc.
Product code	DYB
Device class	Class II
Decision date	Nov 2, 1993
Decision	Substantially Equivalent
Regulation	870.1340

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View the full FDA submission: accessdata.fda.gov

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BURRON CARDIOVASCULAR ANGESTAT(TM)

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