# K922833: Quanta Lite RNP Elisa

- Pathway: 510(k) (Traditional)
- Applicant: Inova Diagnostics, Inc.
- Decided: Sep 18, 1992 after 98 days
- Product code: LLL (Extractable Antinuclear Antibody, Antigen And Control)
- Device class: 2
- Regulation: 21 CFR 866.5100
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 3 cite 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)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K123261: Euroimmun Anti-NRNP/SM Elisa (Igg) (2013), 1 descendant of its own
- K123593: Quanta Flash SM, Quanta Flash RNP, Quanta Flash SM Calibrators, Quanta Flash RNP Calibrators, Quanta Flash SM Controls, (2013), 1 descendant of its own
- K041658: Bioplex 200 Ana Screen on the Bioplex 2200 Multi-Analyte Detection System, Model Bioplex 2200 (2004), 1 descendant of its own
- K213403: Aptiva CTD Essential Reagent (2023), 0 descendants of its own
- K140224: Euroimmun Euroline Ena Profile 9AG (Igg) (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K922833
Methodology: https://510kreport.com/methodology
