DEKA Infusion System, DEKA Administration Set

No FDA recalls on record, checked 22 Oct 2026.

510(k) Number

K242693 ↗

FDA Product Code

LDR

Device Class

Class II

Regulation

21 CFR Part 880.5725

Advisory Committee

General Hospital

FDA Decision

SESE Substantially Equivalent

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  FDA 510(k) K261530 Active Cleared 3 Jun 2026

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  FDA 510(k) K243841 Active Cleared 1 Aug 2025

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  FDA 510(k) K240920 Active Cleared 12 Jul 2024

See all devices from Deka Research and Development →