# K863204: Deka JR.

- Pathway: 510(k) (Traditional)
- Applicant: Deka Research & Development Corp.
- Decided: Sep 3, 1986 after 15 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
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K153760: Volumetric Infusion Controller (2016), 2 descendants of its own
- K232316: DEKA Infusion System, DEKA Administration Set (2024), 1 descendant of its own
- K242693: DEKA Infusion System, DEKA Administration Set (2024), 0 descendants of its own

Source page: https://510kreport.com/device/K863204
Methodology: https://510kreport.com/methodology