K-number	K811238
Device name	MODEL 560 SERIES VOLUMETRIC INFUSION
Applicant	Y
Product code	FRN
Device class	Class II
Decision date	Jun 2, 1981
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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MODEL 560 SERIES VOLUMETRIC INFUSION

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