K-number	K212522
Device name	Lilliput APD System
Applicant	Fresenius Medical Care Renal Therapies Group, LLC
Product code	FKX
Device class	Class II
Decision date	Apr 15, 2022
Decision	Substantially Equivalent
Regulation	876.5630

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Source

View the full FDA submission: accessdata.fda.gov

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Lilliput APD System

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