510(k) Report

510(k) · Cleared

Cleared

Abx Pentra Urine Cal

K071779510(k) AbbreviatedCleared Mar 5, 2008247-day reviewClass II21 CFR 862.1150

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

Horiba Abx · JIX Calibrator, Multi-Analyte Mixture

Cleared on Mar 5, 2008 as substantially equivalent to K050026 (Roche Diagnostics, 2005) after a 247-day review. Its family tree reaches back 5 generations to 1987.

Decided
Mar 5, 2008
Review
247 days
Class
Class II
Product code
JIX
Recalls
None
Predicates
1

Its longest line of descent runs back 5 generations to K871027 (1987). 7 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 5 generations backK871027 Precinorm (R) ProteinBoehringer Mannheim Corp. · 1987
  2. 4 generations backK981401 Boehringer Mannheim Precinorm Precipath Protein ControlsBoehringer Mannheim Corp. · 1998
  3. 3 generations backK040280 Precinorm Proteins in Urine/CSF Precipath Proteins in Urine/CSR…Roche Diagnostics Corp. · 2004
  4. 2 generations backK041812 Modification to Roche Diagnostics Precinorm Proteins in Urine/CSF…Roche Diagnostics Corp. · 2004
  5. 1 generation backK050026 Precinorm Proteins in Urine/CSF (Puc) and Precipath PucRoche Diagnostics · 2005
  6. This deviceK071779 Abx Pentra Urine CalHoriba Abx · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−5K871027Precinorm (R) ProteinBoehringer Mannheim Corp.1987—
−4K981401Boehringer Mannheim Precinorm Precipath Protein ControlsBoehringer Mannheim Corp.1998—
−3K040280Precinorm Proteins in Urine/CSF Precipath Proteins in Urine/CSR ControlsRoche Diagnostics Corp.2004—
−2K041812Modification to Roche Diagnostics Precinorm Proteins in Urine/CSF (Puc) and…Roche Diagnostics Corp.2004—
−1K050026Precinorm Proteins in Urine/CSF (Puc) and Precipath PucRoche Diagnostics2005—
0 (this device)K071779Abx Pentra Urine CalHoriba Abx2008—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199310
200410
FIG. 1 — Lineage of K071779, 1987–2008Source: 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 JIX? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin the report
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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
*K050026Precinorm Proteins in Urine/CSF (Puc) and Precipath Puc
Summary page 1
…Substantially equivalent Submission device Predicate device ABXPENTRAUrine Cal K050026 Section 5-1 Descriptio…
Roche Diagnostics2005—

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 21 years and passes through 4 companies; a new generation was cleared every 3.1 years on median.
  • None of the 7 ancestors has a recall.

How does its category compare?

All JIX devices

JIX Calibrator, Multi-Analyte Mixture: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.

FDA decisions per year · JIX

1in 2016

2007: 62008: 52009: 42010: 52011: 72012: 22013: 42014: 12015: 32016: 1
2007high 7 (2011) · low 0 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · JIX

29in 2015

2007: 53 days median2008: 69 days median2009: 121 days median2010: 100 days median2011: 77 days median2013: 50 days median2015: 29 days median
2007high 121 (2009) · low 29 (2015)2026

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

Recalls per year · JIX

7in 2023

2007: 22008: 32009: 22010: 12011: 22012: 12014: 12016: 12017: 12018: 12019: 12020: 22023: 72026 (partial year): 1
2007high 7 (2023) · low 0 (2013)2026

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

Adverse event reports per year · JIX

18in 2025

2007: 1402008: 1732009: 392011: 92012: 32013: 242014: 352015: 42016: 62017: 172018: 162019: 122020: 222021: 92022: 112023: 132024: 152025: 18
2007high 173 (2008) · low 0 (2010)2025

MAUDE reports naming product code JIX, 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
20076532140
20085693173
20094121239
2010510010
201177729
20122—13
2013450024
20141—135
201532904
20161—16
20170—117
20180—116
20190—112
20200—222
20210—09
20220—011
20230—713
20240—015
20250—018
20260—1—

What is it indicated for?

The ABX PENTRA Urine Cal is a calibrator for use in the calibration of the quantitative method: ABX PENTRA Urinary Proteins CP on Horiba ABX PENTRA 400 clinical chemistry analyzer.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K071779: Abx Pentra Urine Cal.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K071779

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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