510(k) Report

FDA product code · Clinical chemistry

Electrode, Ion-Specific, Chloride

CGZClass II21 CFR 862.1170510(k) required38 decisions since 19798 recalls

38 FDA decisions since 1979. 8 recalls name this code, 0 of them Class I. The most-cited predicate is K000926, 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, clinical chemistry panel

Twenty years of CGZ 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 · CGZ

1in 2018

2007: 12008: 22016: 12017: 12018: 1
2007high 2 (2008) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CGZ

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

Recalls per year · CGZ

2in 2019

2007: 12008: 12009: 12011: 12019: 2
2007high 2 (2019) · low 0 (2010)2026

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

Adverse event reports per year · CGZ

5in 2025

2007: 42009: 12010: 72011: 52012: 302013: 422014: 102015: 22016: 12017: 22018: 192019: 32020: 32022: 52023: 92024: 62025: 5
2007high 42 (2013) · low 0 (2008)2025

MAUDE reports naming product code CGZ, 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—14
20082—10
20090—11
20100—07
20110—15
20120—030
20130—042
20140—010
20150—02
20161—01
20171—02
20181—019
20190—23
20200—03
20210—00
20220—05
20230—09
20240—06
20250—05
20260—0—
FIG. 1 — CGZ by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in CGZ? 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 862.1170.