510(k) Report

510(k) · Cleared

Cleared

Ontrak Testcup 501, Model 3016633

K001421510(k) SpecialCleared Jul 12, 200068-day reviewClass II21 CFR 862.3100

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

Roche Diagnostics Corp. · DKZ Enzyme Immunoassay, Amphetamine

Cleared on Jul 12, 2000 after a 68-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 6 later devices descend from it.

Decided
Jul 12, 2000
Review
68 days
Class
Class II
Product code
DKZ
Recalls
None
Predicates
0

6 later devices descend from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared2006: 1 descendant cleared2015: 1 descendant cleared2016: 1 descendant cleared2023: 1 descendant cleared2026: 1 descendant cleared200020052010201520202025
  1. This deviceK001421 Ontrak Testcup 501, Model 3016633Roche Diagnostics Corp. · 2000
  2. Descendant · cites it directly · 5 of its ownK033902 Ontrak Testcup II and Onsite CupkitVarian, Inc. · 2004
  3. Descendant · 2 generations on · 4 of its ownK060896 Modification to Ontrak Testcup II and Onsite CupkitVarian, Inc. · 2006
  4. Descendant · 3 generations on · 2 of its ownK153192 Chemtrue Multi-Panel Drug Screen Dip Card/Cup Tests, Chemtrue…Chemtron Biotech, Inc. · 2016
  5. Descendant · 4 generations on · 1 of its ownK232736 Chemtrue® Drug Screen Fentanyl/Tramadol Cup Test, Chemtrue® Drug…Chemtron Biotech, Inc. · 2023
  6. Descendant · 5 generations on · 0 of its ownK252684 Labcorp Fentanyl Urine Visual TestMedtox Diagnostics, Inc. · 2026

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2004: 12006: 12015: 12016: 12023: 12026: 1
2004high 1 (2004) · low 0 (2005)2026

Most influential descendants

Showing 5 of 6 · See all
  • K033902Ontrak Testcup II and Onsite CupkitVarian, Inc. · 2004 · cites it directly5descendants
  • K060896Modification to Ontrak Testcup II and Onsite CupkitVarian, Inc. · 2006 · 2 generations on4descendants
  • K153192Chemtrue Multi-Panel Drug Screen Dip Card/Cup Tests, Chemtrue Multi-Panel Drug Screen…Chemtron Biotech, Inc. · 2016 · 3 generations on2descendants
  • K232736Chemtrue® Drug Screen Fentanyl/Tramadol Cup Test, Chemtrue® Drug Screen…Chemtron Biotech, Inc. · 2023 · 4 generations on1descendant
  • K252684Labcorp Fentanyl Urine Visual TestMedtox Diagnostics, Inc. · 2026 · 5 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K001421Ontrak Testcup 501, Model 3016633Roche Diagnostics Corp.2000—
+1K033902Ontrak Testcup II and Onsite CupkitVarian, Inc.2004—
+2K060896Modification to Ontrak Testcup II and Onsite CupkitVarian, Inc.2006—
+3K153192Chemtrue Multi-Panel Drug Screen Dip Card/Cup Tests, Chemtrue Multi-Panel Drug…Chemtron Biotech, Inc.2016—
+4K232736Chemtrue® Drug Screen Fentanyl/Tramadol Cup Test, Chemtrue® Drug Screen…Chemtron Biotech, Inc.2023—
+5K252684Labcorp Fentanyl Urine Visual TestMedtox Diagnostics, Inc.2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
200610
201510
201610
202310
202610
FIG. 1 — Lineage of K001421, 2000–2026Source: 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 DKZ? 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 DKZ device

  1. #1 K233019 AllTest Multi-Drug Rapid Test Cup; AllTest…score 14.6 · 8 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

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? (6)

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

NumberDeviceApplicantDecidedDescendants
K033902Ontrak Testcup II and Onsite CupkitVarian, Inc.20045

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, K033902 (Varian, Inc., 2004) has gone furthest, with 5 descendants of its own.

How does its category compare?

All DKZ devices

DKZ Enzyme Immunoassay, Amphetamine: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DKZ

1in 2024

2008: 22009: 22010: 42011: 62012: 52013: 82014: 82015: 52016: 52018: 32019: 32020: 12023: 22024: 1
2007high 8 (2013) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DKZ

180in 2019

2010: 233 days median2011: 123 days median2012: 55 days median2013: 103 days median2014: 128 days median2015: 107 days median2016: 215 days median2018: 128 days median2019: 180 days median
2007high 233 (2010) · low 55 (2012)2026

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

Recalls per year · DKZ

1in 2017

2007: 12008: 32009: 52011: 42013: 12014: 32017: 1
2007high 5 (2009) · low 0 (2010)2026

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

Adverse event reports per year · DKZ

2in 2025

2008: 122009: 12010: 12011: 22013: 12014: 92015: 82016: 82021: 32022: 42023: 72024: 12025: 2
2007high 12 (2008) · low 0 (2007)2025

MAUDE reports naming product code DKZ, 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
20070—10
20082—312
20092—51
2010423301
2011612342
201255500
2013810311
2014812839
2015510708
2016521508
20170—10
2018312800
2019318000
20201—00
20210—03
20220—04
20232—07
20241—01
20250—02
20260—0—
Cite this page

510(k) Report. “K001421: Ontrak Testcup 501, Model 3016633.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K001421

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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