K-number	K833034
Device name	UNIVERSAL VENTED & NON/VOLUME INFUS-
Applicant	Y
Product code	FPA
Device class	Class II
Decision date	Nov 7, 1983
Decision	Substantially Equivalent
Regulation	880.5440

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View the full FDA submission: accessdata.fda.gov

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UNIVERSAL VENTED & NON/VOLUME INFUS-

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