510(k) Report

FDA product code · Gastroenterology and urology

Strip, Test, Reagent, Residuals For Dialysate, Disinfectant

MSYClass II21 CFR 876.5665510(k) required13 decisions since 19970 recalls

13 FDA decisions since 1997. 510(k) reviews decided 2021–2025 took a median of 101 days (half between 95 and 107). No recall names this code. The most-cited predicate is K983997, named by 1 later device.

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, gastroenterology and urology panel

Twenty years of MSY 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 · MSY

1in 2025

2008: 12009: 12014: 12020: 12022: 12025: 1
2007high 1 (2008) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MSY

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

Recalls per year · MSY

No recall names MSY since 2007.

Adverse event reports per year · MSY

1in 2011

2007: 22008: 352011: 1
2007high 35 (2008) · low 0 (2009)2025

MAUDE reports naming product code MSY, 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—02
20081—035
20091—00
20100—00
20110—01
20120—00
20130—00
20141—00
20150—00
20160—00
20170—00
20180—00
20190—00
20201—00
20210—00
20221—00
20230—00
20240—00
20251—00
20260—0—
FIG. 1 — MSY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in MSY? 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 876.5665.