510(k) Report

FDA product code · Clinical chemistry

Enzymatic Method, Ammonia

JIFClass I21 CFR 862.1065510(k) required30 decisions since 19763 recalls

30 FDA decisions since 1976. 3 recalls name this code, 0 of them Class I. The most-cited predicate is K770363, 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, clinical chemistry panel

Twenty years of JIF 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 · JIF

1in 2019

2013: 22019: 1
2007high 2 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIF

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

Recalls per year · JIF

1in 2015

2007: 12009: 12015: 1
2007high 1 (2007) · low 0 (2008)2026

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

Adverse event reports per year · JIF

5in 2025

2009: 12010: 32011: 72013: 22014: 12015: 32016: 42017: 72018: 12019: 12020: 12021: 12022: 22023: 42024: 12025: 5
2007high 7 (2011) · low 0 (2007)2025

MAUDE reports naming product code JIF, 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—10
20080—00
20090—11
20100—03
20110—07
20120—00
20132—02
20140—01
20150—13
20160—04
20170—07
20180—01
20191—01
20200—01
20210—01
20220—02
20230—04
20240—01
20250—05
20260—0—
FIG. 1 — JIF by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in JIF? 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 862.1065.