510(k) Report

510(k) · Cleared

Cleared

Nichols Advantage Cortisol

K042689510(k) TraditionalCleared Dec 9, 200471-day reviewClass II21 CFR 862.1205

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

Nichols Institute Diagnostics · CGR Radioimmunoassay, Cortisol

Cleared on Dec 9, 2004 as substantially equivalent to K810891 (Diagnostic Products Corp., 1981) after a 71-day review. Its family tree reaches back 1 generation to 1981.

Decided
Dec 9, 2004
Review
71 days
Class
Class II
Product code
CGR
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K810891 (1981). No later device cites it as a predicate yet.

K810891 · Coat-a-Count Cortisol Ria Kit · Diagnostic Products Corp. · 1981198019851990199520002005
  1. Root · 1 generation backK810891 Coat-a-Count Cortisol Ria KitDiagnostic Products Corp. · 1981
  2. This deviceK042689 Nichols Advantage CortisolNichols Institute Diagnostics · 2004
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K810891Coat-a-Count Cortisol Ria KitDiagnostic Products Corp.1981—
0 (this device)K042689Nichols Advantage CortisolNichols Institute Diagnostics2004—
FIG. 1 — Lineage of K042689, 1981–2004Source: 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 CGR? 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 CGR device

  1. #1 K242190 Access Cortisol; DxC 500i Clinical Analyzerscore 7.3 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin 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
*K810891Coat-a-Count Cortisol Ria Kit
Summary page 1
…d. 6. Comparison to Predicate Device: The Nichols Advantage Cortisol (Y) was compared to the DPC Coat-A-Count Cortisol RIA (X) previously cleared by the FDA (K810891, 4/14/81). One hundred fifty (150) serum samples in which the clinical diagnosis were unknown were assayed in duplicate by…
Diagnostic Products Corp.1981—

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?

  • Its one ancestor has no recall.

How does its category compare?

All CGR devices

CGR Radioimmunoassay, Cortisol: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CGR

1in 2025

2021: 32023: 12025: 1
2007high 3 (2021) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CGR

113in 2021

2021: 113 days median
2007high 113 (2021)2026

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

Recalls per year · CGR

2in 2025

2009: 12010: 12014: 12024: 12025: 2
2007high 2 (2025) · low 0 (2007)2026

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

Adverse event reports per year · CGR

1in 2018

2009: 12010: 12011: 22014: 22018: 1
2007high 2 (2011) · low 0 (2007)2025

MAUDE reports naming product code CGR, 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—00
20080—00
20090—11
20100—11
20110—02
20120—00
20130—00
20140—12
20150—00
20160—00
20170—00
20180—01
20190—00
20200—00
2021311300
20220—00
20231—00
20240—10
20251—20
20260—0—

What is it indicated for?

The Nichols Advantage® Cortisol assay is intended for use with the Nichols Advantage® Specialty System for the quantitative determination of cortisol concentrations in human serum, EDTA plasma and urine. Measurements of cortisol are used in the diagnosis and treatment of disorders of the adrenal gland.

The Nichols Advantage Cortisol Assay Calibrators are intended for adjustment of the stored curve for the Nichols Advantage Cortisol assay.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K042689: Nichols Advantage Cortisol.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K042689

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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