K-number	K780130
Device name	BURETTE INTRAVENOUS ADMIN. SETS.
Applicant	Y
Product code	FPA
Device class	Class II
Decision date	Feb 21, 1978
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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BURETTE INTRAVENOUS ADMIN. SETS.

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