# K242693: DEKA Infusion System, DEKA Administration Set

- Pathway: 510(k) (Special)
- Applicant: Deka Research and Development Corporation
- Decided: Oct 7, 2024 after 28 days
- Product code: LDR (Controller, Infusion, Intravascular, Electronic)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 4 generations back to K832284 (1983). 8 ancestors in all.
No later device cites it as a predicate yet.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232316: DEKA Infusion System, DEKA Administration Set, Deka Research and Development (2024) Summary page 6.

## Indications for use
The DEKA Infusion System is indicated for continuous delivery of general maintenance fluids and supported antibiotics to adult patients through a peripheral intravenous (IV) site under the supervision of a qualified clinician.

Source page: https://510kreport.com/device/K242693
Methodology: https://510kreport.com/methodology