# K132874: Lumencare Azure Set F6, 150CM, Lumecare Azure Set 5F, 150 CM, Lumencare Azure Set 5F, 140 CM

- Pathway: 510(k) (Special)
- Applicant: Nucletron B.V.
- Decided: Feb 21, 2014 after 161 days
- Product code: JAQ (System, Applicator, Radionuclide, Remote-Controlled)
- Device class: 2
- Regulation: 21 CFR 892.5700
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Lumencath Applicator Set: named in the summary without a submission number

## Most influential descendants
- K262383: LumenCare Azure (2026), 0 descendants of its own

## Indications for use
The LumenCare Azure is intended for intraluminal brachytherapy and is used for treatment of the lung or other lumen, e.g. bronchus and bile duct. The LumenCare Azure is designed to fit in the working channel of an endoscope.

Source page: https://510kreport.com/device/K132874
Methodology: https://510kreport.com/methodology