K-number	K240624
Device name	InfuLife
Applicant	First Medical Source, LLC
Product code	MEB
Device class	Class II
Decision date	Nov 5, 2024
Decision	Substantially Equivalent
Regulation	880.5725

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Source

View the full FDA submission: accessdata.fda.gov

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InfuLife

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