# K922737: Vidas Toxo IG6 Assay (TX6)

- Pathway: 510(k) (Traditional)
- Applicant: Biomerieux Vitek, Inc.
- Decided: May 11, 1993 after 337 days
- Product code: LGD (Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii)
- Device class: 2
- Regulation: 21 CFR 866.3780
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K012183: Bayer Diagnostics Advia Centaur Toxoplasma Igg Assay (2001), 1 descendant of its own
- K102681: Advia Centaur Toxoplasma Igg (Toxo G) (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K922737
Methodology: https://510kreport.com/methodology