510(k) Report

FDA product code · Microbiology

Antigens, All Groups, Streptococcus Spp.

GTYClass I21 CFR 866.3740510(k) exempt44 decisions since 19816 recalls

FDA lists GTY 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. 44 FDA decisions since 1981. 510(k) reviews decided 2021–2025 took a median of 194 days (half between 185 and 202). 6 recalls name this code, 0 of them Class I. The most-cited predicate is K133343, named by 2 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 GTY 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 · GTY

1in 2025

2008: 12009: 12013: 22014: 22017: 12022: 12025: 12026 (partial year): 1
2007high 2 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GTY

Too few GTY 510(k)s in any year since 2007 to give a median.

Recalls per year · GTY

4in 2011

2011: 42026 (partial year): 1
2007high 4 (2011) · low 0 (2007)2026

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

Adverse event reports per year · GTY

94in 2025

2007: 12008: 22009: 22010: 12011: 32014: 12015: 12017: 22018: 122019: 62020: 12021: 372022: 322023: 442024: 412025: 94
2007high 94 (2025) · low 0 (2012)2025

MAUDE reports naming product code GTY, 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
20070—01
20081—02
20091—02
20100—01
20110—43
20120—00
20132—00
20142—01
20150—01
20160—00
20171—02
20180—012
20190—06
20200—01
20210—037
20221—032
20230—044
20240—041
20251—094
20261—1—
FIG. 1 — GTY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in GTY? 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 866.3740.