510(k) Report

510(k) · Cleared

Cleared

Nano-Check™ RSV Test

K240280510(k) Dual TrackCleared Jul 30, 2024180-day reviewClass I21 CFR 866.3480

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Nano-Ditech Corporation · GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

Cleared on Jul 30, 2024 after a 180-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Jul 30, 2024
Review
180 days
Class
Class I
Product code
GQG
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2026: 1 descendant cleared2020202220242026
  1. This deviceK240280 Nano-Check™ RSV TestNano-Ditech Corporation · 2024
  2. Descendant · cites it directly · 0 of its ownK253318 Clungene RSV Antigen Rapid TestHangzhou Clongene Biotech Co., Ltd. · 2026

Most influential descendants

Showing 1 of 1 · See all
  • K253318Clungene RSV Antigen Rapid TestHangzhou Clongene Biotech Co., Ltd. · 2026 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K240280Nano-Check™ RSV TestNano-Ditech Corporation2024—
+1K253318Clungene RSV Antigen Rapid TestHangzhou Clongene Biotech Co., Ltd.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202610
FIG. 1 — Lineage of K240280, 2024–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in GQG? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new GQG device

  1. #1 K253318 Clungene RSV Antigen Rapid Testscore 10.8 · 1 generation · no Class I recall
Get a 510(k) Report

What was it cleared against?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K253318Clungene RSV Antigen Rapid TestHangzhou Clongene Biotech Co., Ltd.20260

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

What does this lineage say?

  • Of its descendants, K253318 (Hangzhou Clongene Biotech Co., Ltd., 2026) has gone furthest, with 0 descendants of its own.

How does its category compare?

All GQG devices

GQG Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus: FDA decisions, review times, recalls and adverse event reports over 20 years. 2024, this device’s year, is highlighted.

FDA decisions per year · GQG

1in 2024

2007: 12009: 12010: 22012: 12013: 32017: 12024: 12026 (partial year): 1
2007high 3 (2013) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GQG

93in 2013

2013: 93 days median
2007high 93 (2013)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · GQG

1in 2007

2007: 1
2007high 1 (2007) · low 0 (2008)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · GQG

2in 2025

2009: 12018: 12020: 12021: 52022: 32023: 62024: 22025: 2
2007high 6 (2023) · low 0 (2007)2025

MAUDE reports naming product code GQG, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—10
20080—00
20091—01
20102—00
20110—00
20121—00
201339300
20140—00
20150—00
20160—00
20171—00
20180—01
20190—00
20200—01
20210—05
20220—03
20230—06
20241—02
20250—02
20261—0—
Cite this page

510(k) Report. “K240280: Nano-Check™ RSV Test.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K240280

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026