# K071219: Athena Multi-Lyte GBM Test System

- Pathway: 510(k) (Traditional)
- Applicant: Zeus Scientific, Inc.
- Decided: Dec 6, 2007 after 218 days
- Product code: MVJ (Devices, Measure, Antibodies To Glomerular Basement Membrane (Gbm))
- Device class: 2
- Regulation: 21 CFR 866.5660
- 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. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K261466: Alegria Flash MPO; Alegria Flash PR3; Alegria Flash GBM (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K071219
Methodology: https://510kreport.com/methodology