# K152157: LC Bead LUMI

- Pathway: 510(k) (Traditional)
- Applicant: Biocompatibles UK, Ltd.
- Decided: Dec 11, 2015 after 130 days
- Product code: KRD (Device, Vascular, For Promoting Embolization)
- Device class: 2
- Regulation: 21 CFR 870.3300
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 5 generations back to K010026 (2001). 5 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083091: LC Bead Microspheres, Bead Block Compressible Microspheres, Biocompatibles UK Limited (2008) Summary page 4.

## Most influential descendants
- K162373: LC Bead LUMI (2016), 0 descendants of its own

## Indications for use
LC Bead LUMI are intended to be used for the embolization of hypervascular tumors and arteriovenous malformations (AVMs).

Source page: https://510kreport.com/device/K152157
Methodology: https://510kreport.com/methodology