510(k) Report

FDA product code · Microbiology

Antigen, Cf (Including Cf Controls), Respiratory Syncytial Virus

GQGClass I21 CFR 866.3480510(k) exempt32 decisions since 19773 recalls

FDA lists GQG as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 866.9 applies, such as a new intended use or a different fundamental technology. 32 FDA decisions since 1977. 510(k) reviews decided 2021–2025 took a median of 180 days (half between 180 and 180). 3 recalls name this code, 0 of them Class I. The most-cited predicate is K882629, named by 4 later devices.

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

FIG. A — Illustration, microbiology panel

Twenty years of GQG at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

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—
FIG. 1 — GQG by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in GQG? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Related product codes

Other codes under 21 CFR 866.3480.