K-number	K791531
Device name	FLEXIFLO ENTERAL PUMP SET
Applicant	Abbott Laboratories
Product code	BSS
Device class	Class II
Decision date	Sep 12, 1979
Decision	Substantially Equivalent
Regulation	876.5980

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Source

View the full FDA submission: accessdata.fda.gov

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FLEXIFLO ENTERAL PUMP SET

Everything you need for a 510(k) submission. Nothing you don't.