K-number	K242693
Device name	DEKA Infusion System, DEKA Administration Set
Applicant	Deka Research and Development Corporation
Product code	LDR
Device class	Class II
Decision date	Oct 7, 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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