510(k) Report

510(k) · Cleared

Cleared

Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions

K253490510(k) TraditionalCleared Feb 12, 2026111-day reviewClass II21 CFR 862.1345

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

Roche Diagnostics · CFR Hexokinase, Glucose

Cleared on Feb 12, 2026 as substantially equivalent to K191899 (Roche Diagnostics, 2019) and 1 other predicate after a 111-day review. Its family tree reaches back 3 generations to 1993.

Decided
Feb 12, 2026
Review
111 days
Class
Class II
Product code
CFR
Recalls
None
Predicates
2

Its longest line of descent runs back 3 generations to K930928 (1993). 8 ancestors in all. No later device cites it as a predicate yet.

Other ancestors, by year cleared 2019: 2 other ancestors2006: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestorK930928 · Roche Abuscreen Online for Methadone · Roche Diagnostic Systems, Inc. · 1993K983703 · Modification to Abuscreen Online for Methadone · Roche Diagnostic Systems, Inc. · 1998K021505 · Online Dat II Methadone II · Roche Diagnostics Corp. · 20021990200020102020
Other ancestors, by generation 1 generation back: 1 other ancestor2 generations back: 2 other ancestors3 generations back: 2 other ancestors K021505 · Online Dat II Methadone II · Roche Diagnostics Corp. · 2002K983703 · Modification to Abuscreen Online for Methadone · Roche Diagnostic Systems, Inc. · 1998K930928 · Roche Abuscreen Online for Methadone · Roche Diagnostic Systems, Inc. · 19930
  1. Root · 3 generations backK930928 Roche Abuscreen Online for MethadoneRoche Diagnostic Systems, Inc. · 1993
  2. 2 generations backK983703 Modification to Abuscreen Online for MethadoneRoche Diagnostic Systems, Inc. · 1998
  3. 1 generation backK021505 Online Dat II Methadone IIRoche Diagnostics Corp. · 2002
  4. This deviceK253490 Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated…Roche Diagnostics · 2026
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−3K930928Roche Abuscreen Online for MethadoneRoche Diagnostic Systems, Inc.1993—
−2K983703Modification to Abuscreen Online for MethadoneRoche Diagnostic Systems, Inc.1998—
−1K021505Online Dat II Methadone IIRoche Diagnostics Corp.2002—
0 (this device)K253490Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutionsRoche Diagnostics2026—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
200610
201920
FIG. 1 — Lineage of K253490, 1993–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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 CFR? 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 CFR device

  1. #1 K252357 Glucose2score 10.5 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (2)

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
*K191899Glucose HK Gen.3, ISE indirect Na for Gen.2, Elecsys TSH, cobas pro integrated solutions
Summary page 7
…cobas c 703 in cobas pro integrated solutions integrated solutions (K191899) (K253490) Fully automated clinical…
Roche Diagnostics20193
*K021505Online Dat II Methadone II
Summary page 11
…Roche/Hitachi Family cobas c 703 (K253490) (K021505) Methodology KIMS, Kinetic interaction of Same…
Roche Diagnostics Corp.2002—

Also cleared against K191899: 2 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 33 years and passes through 3 companies; a new generation was cleared every 5.2 years on median.
  • 4 of the 8 ancestors have a recall of any class.
  • 2 other devices also cite its predicate K191899.

How does its category compare?

All CFR devices

CFR Hexokinase, Glucose: FDA decisions, review times, recalls and adverse event reports over 20 years. 2026, this device’s year, is highlighted.

FDA decisions per year · CFR

1in 2025

2007: 12008: 52009: 32011: 32012: 42013: 12014: 12016: 22017: 12019: 12022: 12025: 12026 (partial year): 1
2007high 5 (2008) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CFR

115in 2012

2008: 182 days median2009: 101 days median2011: 316 days median2012: 115 days median
2007high 316 (2011) · low 101 (2009)2026

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

Recalls per year · CFR

1in 2016

2008: 72009: 12012: 12014: 12016: 1
2007high 7 (2008) · low 0 (2007)2026

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

Adverse event reports per year · CFR

16in 2025

2007: 12008: 22009: 72010: 112011: 432012: 492013: 362014: 22015: 32016: 12017: 132018: 82019: 102020: 42021: 52022: 32023: 292024: 152025: 16
2007high 49 (2012) · low 1 (2007)2025

MAUDE reports naming product code CFR, 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
2008518272
2009310117
20100—011
20113316043
20124115149
20131—036
20141—12
20150—03
20162—11
20171—013
20180—08
20191—010
20200—04
20210—05
20221—03
20230—029
20240—015
20251—016
20261—0—

What is it indicated for?

cobas pro integrated solutions is an automated analyzer, intended for running qualitative, semiquantitative, and quantitative clinical chemistry and immunochemistry assays as well as ion-selective measurements. Glucose HK Gen.3 is an in vitro test for the quantitative determination of glucose in human serum, plasma, urine and CSF on cobas c systems. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders…

Read the full statement (204 words)

cobas pro integrated solutions is an automated analyzer, intended for running qualitative, semiquantitative, and quantitative clinical chemistry and immunochemistry assays as well as ion-selective measurements.

Glucose HK Gen.3 is an in vitro test for the quantitative determination of glucose in human serum, plasma, urine and CSF on cobas c systems. Glucose measurements are used in the diagnosis and treatment of carbohydrate metabolism disorders including diabetes mellitus, neonatal hypoglycemia, and idiopathic hypoglycemia, and pancreatic islet cell tumors.

Methadone II (MDN2) is an in vitro diagnostic test for the qualitative and semiquantitative detection of methadone in human urine on cobas c systems at a cutoff concentration of 300 ng/mL. Semiquantitative test results may be obtained that permit laboratories to assess assay performance as part of a quality control program. Semiquantitative assays are intended to determine an appropriate dilution of the specimen for confirmation by a confirmatory method such as gas chromatography/masspectrometry (GC-MS).

Methadone 1I provides only a preliminary analytical test result. A more specific alternate chemical method must be used in order to obtain a confirmed analytical result. GC-MS is the preferred confirmatory method. Clinical consideration and professional judgment should be applied to any drug of abuse test result, particularly when preliminary positive results are used.

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. “K253490: Glucose HK Gen.3; ONLINE DAT Methadone II; cobas pro integrated solutions.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K253490

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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