510(k) Report

510(k) · Cleared

Cleared

DUS R-50S (Urine Chemistry system)

K171521510(k) TraditionalCleared Feb 16, 2018268-day reviewClass II21 CFR 862.1340

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

DFI Co., Ltd. · JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative)

Cleared on Feb 16, 2018 as substantially equivalent to K091216 (Siemens Healthcare Diagnostics, 2009) after a 268-day review. Its family tree reaches back 3 generations to 1991.

Decided
Feb 16, 2018
Review
268 days
Class
Class II
Product code
JIL
Recalls
None
Predicates
1

Its longest line of descent runs back 3 generations to K905396 (1991). 9 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2003: 2 other ancestors2002: 1 other ancestor1999: 1 other ancestor1997: 1 other ancestor1996: 1 other ancestorK905396 · 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 · recalled1990199520002005201020152020
  1. Root · 3 generations backK905396 Hemastix Reagent StripsHeraeus Kulzer, Inc. · 1991
  2. 2 generations backK031947 Bayer Clinitek Status AnalyzerBayer Healthcare, LLC · 2003
  3. 1 generation backK091216 Clinitek Status+Analyzer and Clinitek Status Connect System, Models…Siemens Healthcare Diagnostics · 2009 · Recalled
  4. This deviceK171521 DUS R-50S (Urine Chemistry system)DFI Co., Ltd. · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K905396Hemastix Reagent StripsHeraeus Kulzer, Inc.1991—
−2K031947Bayer Clinitek Status AnalyzerBayer Healthcare, LLC2003—
−1K091216Clinitek Status+Analyzer and Clinitek Status Connect System, Models 1780, 1797Siemens Healthcare Diagnostics20094
0 (this device)K171521DUS R-50S (Urine Chemistry system)DFI Co., Ltd.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
199710
199910
200210
200320
FIG. 1 — Lineage of K171521, 1991–2018Source: 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 JIL? 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 JIL device

  1. #1 K193514 AUTION MAX AX-4060 Urinalysis Systemscore 6.1 · 4 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
*K091216Clinitek Status+Analyzer and Clinitek Status Connect System, Models 1780, 1797
Summary page 5
…862.1115 JJB I (nonquantitative) test system Automated Urinalysis System 21 CFR 862.2900 KQO I Predicate Device Information: K091216 / Clinitek Status+ Device Description: The DUS R-50S (Urine Chemistry system) is a portable analyzer. It is designed to read on…
Siemens Healthcare Diagnostics20094

Also cleared against K091216: 3 other devices →

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.

What does this lineage say?

  • The line of descent spans 27 years and passes through 4 companies; a new generation was cleared every 8.4 years on median.
  • 3 of the 9 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K091216.

How does its category compare?

All JIL devices

JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative): FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · JIL

1in 2023

2007: 32009: 12011: 12012: 12014: 12015: 12016: 22017: 12018: 42019: 12023: 1
2007high 4 (2018) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIL

187in 2018

2007: 284 days median2018: 187 days median
2007high 284 (2007) · low 187 (2018)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · JIL

1in 2025

2014: 42016: 12025: 1
2007high 4 (2014) · low 0 (2007)2026

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

Adverse event reports per year · JIL

15in 2025

2007: 202008: 202009: 162010: 112011: 142012: 52013: 322014: 472015: 452016: 402017: 332018: 682019: 672020: 232021: 122022: 142023: 152024: 212025: 15
2007high 68 (2018) · low 5 (2012)2025

MAUDE reports naming product code JIL, 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
20073284020
20080—020
20091—016
20100—011
20111—014
20121—05
20130—032
20141—447
20151—045
20162—140
20171—033
20184187068
20191—067
20200—023
20210—012
20220—014
20231—015
20240—021
20250—115
20260—0—

What is it indicated for?

The DUS R-50S System provides a qualitative and semi-quantitative measurements for specific gravity, pH, leukocytes, nitrite, protein, glucose, ketone, urobilinogen, bilirubin, blood, microalbumin and creatinine in urine specimens. These measurements are used to aid in the diagnosis of metabolic disorders, kidney function anomalies, urinary tract infections and liver function. The system is intended for prescription, in vitro diagnostic use only. The DUS…

Read the full statement (107 words)

The DUS R-50S System provides a qualitative and semi-quantitative measurements for specific gravity, pH, leukocytes, nitrite, protein, glucose, ketone, urobilinogen, bilirubin, blood, microalbumin and creatinine in urine specimens. These measurements are used to aid in the diagnosis of metabolic disorders, kidney function anomalies, urinary tract infections and liver function. The system is intended for prescription, in vitro diagnostic use only.

The DUS R-50S System consists of the following:

DUS R-50S Analyzer

DUS 10 Reagent Strips for urinalysis include test pads for leukocytes, nitrite, urobilinogen, protein, pH, blood, specific gravity, ketone(acetoacetic acid), bilirubin and glucose.

DUS 2AC Reagent Strips for urinalysis include test pads for microalbumin and creatinine.

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. “K171521: DUS R-50S (Urine Chemistry system).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K171521

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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