K-number	K232316
Device name	DEKA Infusion System, DEKA Administration Set
Applicant	Deka Research and Development
Product code	LDR
Device class	Class II
Decision date	Mar 1, 2024
Decision	Substantially Equivalent
Regulation	880.5725

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View the full FDA submission: accessdata.fda.gov

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DEKA Infusion System, DEKA Administration Set

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