510(k) Report

510(k) · Cleared

Cleared

Immunodip Urinary Albumin Screen Assay, Catalogue Number 790-25

K022538510(k) SpecialCleared Aug 23, 200222-day reviewClass I21 CFR 862.1645

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

Diagnostic Chemicals, Ltd. (Usa) · JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Cleared on Aug 23, 2002 after a 22-day review. FDA’s file for it is a 510(k) statement, which names no predicate.

Decided
Aug 23, 2002
Review
22 days
Class
Class I
Product code
JIR
Recalls
None
Predicates
0

FDA’s file for it is a 510(k) statement, which names no predicate.

FIG. 1 — Lineage of K022538Source: FDA 510(k) database · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in JIR? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new JIR device

  1. #1 K210069 Minuteful - kidney testscore 7.5 · 4 generations · no Class I recall
  2. #2 Held for the reportin the report
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What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All JIR devices

JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.): FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · JIR

1in 2023

2007: 12015: 12022: 12023: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIR

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

Recalls per year · JIR

2so far in 2026, the most since 2007

2026 (partial year): 2
2007high 2 (2026) · low 0 (2007)2026

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

Adverse event reports per year · JIR

2in 2025

2007: 12010: 12011: 12013: 92015: 42016: 52017: 22019: 12020: 22021: 12023: 22024: 42025: 2
2007high 9 (2013) · low 0 (2008)2025

MAUDE reports naming product code JIR, 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—01
20080—00
20090—00
20100—01
20110—01
20120—00
20130—09
20140—00
20151—04
20160—05
20170—02
20180—00
20190—01
20200—02
20210—01
20221—00
20231—02
20240—04
20250—02
20260—2—

What is it indicated for?

For IN VITRO diagnostic use. There are several kidney disease conditions that can produce high levels of albumin in urine (1). Determining albumin in the urine at the low levels measured by this test is helpful for early detection and treatment of patients at risk for renal (kidney) disease. Low but elevated urinary albumin levels, or microalbuminuria, refers to a level of the human protein albumin in urine above about 10 mg/L. Levels above 18 mg/L are…

Read the full statement (217 words)

For IN VITRO diagnostic use.

There are several kidney disease conditions that can produce high levels of albumin in urine (1). Determining albumin in the urine at the low levels measured by this test is helpful for early detection and treatment of patients at risk for renal (kidney) disease. Low but elevated urinary albumin levels, or microalbuminuria, refers to a level of the human protein albumin in urine above about 10 mg/L. Levels above 18 mg/L are not normally found in healthy individuals. These low but significant levels are not detectable with older dipstick assays. The ImmunoDip Urinary Albumin Test classifies samples as positive or negative based on their being above or below a level of 18 mg/L.

Conditions in which elevated levels of albumin in urine may be present include: Type 1 and Type 2 diabetes (2-8); hypertension (9; 10); and renal disease found in pregnancy (11). There are other less common causes as well. Diabetes is the largest single cause. One study found 45% of the insulin-dependent diabetics develop serious kidney disease (3). Testing for elevated levels of albumin in urine helps to identify those diabetics who are prone to kidney disease. Scientific studies indicate that proper control of blood glucose (blood sugar) levels and blood pressure help slow or prevent kidney damage (1, 9).

Indications for use as stated in the FDA 510(k) statement.

Cite this page

510(k) Report. “K022538: Immunodip Urinary Albumin Screen Assay, Catalogue Number 790-25.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K022538

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026