# K240280: Nano-Check™ RSV Test

- Pathway: 510(k) (Dual Track)
- Applicant: Nano-Ditech Corporation
- Decided: Jul 30, 2024 after 180 days
- Product code: GQG (Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus)
- Device class: 1
- Regulation: 21 CFR 866.3480
- 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 has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K253318: Clungene RSV Antigen Rapid Test (2026), 0 descendants of its own

Source page: https://510kreport.com/device/K240280
Methodology: https://510kreport.com/methodology