K-number	K212445
Device name	freeflex+ Transfer Adapter
Applicant	Fresenius Kabi AG
Product code	LHI
Device class	Class II
Decision date	Jun 1, 2022
Decision	Substantially Equivalent
Regulation	880.5440

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Source

View the full FDA submission: accessdata.fda.gov

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freeflex+ Transfer Adapter

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