# K902925: Vitek Immunodiagnostic Assay System (Vidas) (RBG)

- Pathway: 510(k) (Traditional)
- Applicant: Vitek Systems, Inc.
- Decided: Aug 9, 1990 after 37 days
- Product code: LFX (Enzyme Linked Immunoabsorbent Assay, Rubella)
- Device class: 2
- Regulation: 21 CFR 866.3510
- 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
- K080008: Bioplex 2200 System Torc Igg Kit, Calibrator Set and Control Set (2009), 1 descendant of its own
- K120572: Bioplex 2200 Torc Igg (2012), 0 descendants of its own

Source page: https://510kreport.com/device/K902925
Methodology: https://510kreport.com/methodology