510(k) Report

510(k) · Cleared

Cleared

Minuteful - kidney test

K210069510(k) TraditionalCleared Jul 6, 2022541-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

Healthy.Io, Ltd. · JIR Indicator Method, Protein Or Albumin (Urinary, Non-Quant.)

Cleared on Jul 6, 2022 as substantially equivalent to K141874 (Yd Diagnostics Corp., 2015) after a 541-day review. Its family tree reaches back 4 generations to 1991. 1 later device descends from it.

Decided
Jul 6, 2022
Review
541 days
Class
Class I
Product code
JIR
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K905396 (1991). 10 ancestors in all. 1 later device descends from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2003: 2 other ancestors2002: 1 other ancestor1999: 1 other ancestor1997: 1 other ancestor1996: 1 other ancestor2023: 1 descendant clearedK905396 · Hemastix Reagent Strips · Heraeus Kulzer, Inc. · 1991K031947 · Bayer Clinitek Status Analyzer · Bayer Healthcare, LLC · 2003K091216 · Clinitek Status+Analyzer and Clinitek Status Connect System, Models 1780, 1797 · Siemens Healthcare Diagnostics · 2009 · recalledK141874 · Uriscan Optima · Yd Diagnostics Corp. · 20151990200020102020
  1. Root · 4 generations backK905396 Hemastix Reagent StripsHeraeus Kulzer, Inc. · 1991
  2. 3 generations backK031947 Bayer Clinitek Status AnalyzerBayer Healthcare, LLC · 2003
  3. 2 generations backK091216 Clinitek Status+Analyzer and Clinitek Status Connect System, Models…Siemens Healthcare Diagnostics · 2009 · Recalled
  4. 1 generation backK141874 Uriscan OptimaYd Diagnostics Corp. · 2015
  5. This deviceK210069 Minuteful - kidney testHealthy.Io, Ltd. · 2022
  6. Descendant · cites it directly · 0 of its ownK222921 Minuteful-kidney testHealthy.Io, Ltd. · 2023

Most influential descendants

Showing 1 of 1 · See all
  • K222921Minuteful-kidney testHealthy.Io, Ltd. · 2023 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K905396Hemastix Reagent StripsHeraeus Kulzer, Inc.1991—
−3K031947Bayer Clinitek Status AnalyzerBayer Healthcare, LLC2003—
−2K091216Clinitek Status+Analyzer and Clinitek Status Connect System, Models 1780, 1797Siemens Healthcare Diagnostics20094
−1K141874Uriscan OptimaYd Diagnostics Corp.2015—
0 (this device)K210069Minuteful - kidney testHealthy.Io, Ltd.2022—
+1K222921Minuteful-kidney testHealthy.Io, Ltd.2023—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199910
200210
200320

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202310
FIG. 1 — Lineage of K210069, 1991–2023Source: FDA 510(k) summaries, read by 510(k) Report · 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 summary (predicates and 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 K222921 Minuteful-kidney testscore 7.2 · 5 generations · no Class I recall
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What was it cleared against? (1)

Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.

TypeNumberDeviceApplicantDecidedRecalls
*K141874Uriscan Optima
Summary page 5
…anufacturer Device 510(k) Number YD Diagnostics Corp. URiSCAN Optima urine chemistry test system K141874 Device Description: The Minuteful - kidney test is comprised of a kit and a smartphone application. It is intended for the sem…
Yd Diagnostics Corp.2015—

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K222921Minuteful-kidney testHealthy.Io, Ltd.20230

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.

What does this lineage say?

  • The line of descent spans 31 years and passes through 5 companies; a new generation was cleared every 7.1 years on median.
  • 3 of the 10 ancestors have a recall of any class.
  • Of its descendants, K222921 (Healthy.Io, Ltd., 2023) has gone furthest, with 0 descendants of its own.

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. 2022, this device’s year, is highlighted.

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?

The Minuteful — kidney test is an in-vitro diagnostic, home-use urine analysis test system for the semi-quantitative

measurement of albumin and creatinine in urine, as well as the presentation of their ratio, the albumin-creatinine ratio

(ACR). The system consists of a smartphone application, proprietary Color-Board and an ACR Reagent Strip. The system

is available for prescription-use only and is intended for people at risk of kidney disease. Results are intended to be used

in conjunction with clinical evaluation as an aid in the assessment of kidney health.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K210069: Minuteful - kidney test.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210069

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