510(k) Report

510(k) · Cleared

Cleared

Behring Rapignost Total Screen L Urine Test Strips

K861255510(k) TraditionalCleared Oct 3, 1986183-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

Behring Diagnostics, Inc. · JIL Method, Enzymatic, Glucose (Urinary, Non-Quantitative)

Cleared on Oct 3, 1986 after a 183-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 5 later devices descend from it.

Decided
Oct 3, 1986
Review
183 days
Class
Class II
Product code
JIL
Recalls
None
Predicates
0

5 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2006: 1 descendant cleared2009: 1 descendant cleared2012: 1 descendant cleared2024: 1 descendant cleared1990200020102020
  1. This deviceK861255 Behring Rapignost Total Screen L Urine Test StripsBehring Diagnostics, Inc. · 1986
  2. Descendant · cites it directly · 3 of its ownK040703 Uristik H Series Reagent Strips for UrinalysisDirui Industrial Co., Ltd. · 2004
  3. Descendant · 2 generations on · 1 of its ownK082811 Uritest 10G & 11G Urine Reagent Strips and Uritest-50 and…Urit Medical Electronic Co., Ltd. · 2009
  4. Descendant · 3 generations on · 0 of its ownK232317 UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips…Urit Medical Electronic Co., Ltd. · 2024
  5. Descendant · 2 generations on · 0 of its ownK111999 Healgen 11 Reagent Strip for Urinalysis, Healgen 10 Reagent Strip…Healgen Scientific,, LLC · 2012 · Recalled
  6. Descendant · cites it directly · 0 of its ownK061559 Acon Urinalysis Reagent StripsAcon Laboratories Co. · 2006 · Recalled

Most influential descendants

Showing 5 of 5 · See all
  • K040703Uristik H Series Reagent Strips for UrinalysisDirui Industrial Co., Ltd. · 2004 · cites it directly3descendants
  • K082811Uritest 10G & 11G Urine Reagent Strips and Uritest-50 and Uritest-500B Urine AnalyzersUrit Medical Electronic Co., Ltd. · 2009 · 2 generations on1descendant
  • K232317UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA Urine…Urit Medical Electronic Co., Ltd. · 2024 · 3 generations on0descendants
  • K111999Healgen 11 Reagent Strip for Urinalysis, Healgen 10 Reagent Strip for Urinalysis, and…Healgen Scientific,, LLC · 2012 · 2 generations on0descendants
  • K061559Acon Urinalysis Reagent StripsAcon Laboratories Co. · 2006 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K861255Behring Rapignost Total Screen L Urine Test StripsBehring Diagnostics, Inc.1986—
+1K040703Uristik H Series Reagent Strips for UrinalysisDirui Industrial Co., Ltd.2004—
+2K082811Uritest 10G & 11G Urine Reagent Strips and Uritest-50 and Uritest-500B Urine…Urit Medical Electronic Co., Ltd.2009—
+3K232317UC-1800 Automatic Urine Analyzer, URIT 11FA Urine Reagent Strips, URIT 12FA…Urit Medical Electronic Co., Ltd.2024—
+2K111999Healgen 11 Reagent Strip for Urinalysis, Healgen 10 Reagent Strip for…Healgen Scientific,, LLC20121
+1K061559Acon Urinalysis Reagent StripsAcon Laboratories Co.20061

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200610
200910
201210
202410
FIG. 1 — Lineage of K861255, 1986–2024Source: 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), 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?

FDA has not posted a summary or statement for it, so its predicates are not known.

What descends from it? (5)

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K040703Uristik H Series Reagent Strips for UrinalysisDirui Industrial Co., Ltd.20043
K061559Acon Urinalysis Reagent StripsAcon Laboratories Co.20060

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?

  • Of its descendants, K040703 (Dirui Industrial Co., Ltd., 2004) has gone furthest, with 3 descendants of its own.

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.

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—
Cite this page

510(k) Report. “K861255: Behring Rapignost Total Screen L Urine Test Strips.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K861255

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Record history
  • FDA decision record loaded May 2, 2026
  • Lineage and recalls computed Nov 3, 2026
  • Page last updated Nov 3, 2026