510(k) Report

510(k) · Cleared

Cleared

Coat-a-Count Cortisol Ria Kit

K810891510(k) TraditionalCleared Apr 14, 198112-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

Diagnostic Products Corp. · CGR Radioimmunoassay, Cortisol

Cleared on Apr 14, 1981 after a 12-day review. FDA has not posted a summary or statement for it, so its predicates are not known. 1 later device descends from it.

Decided
Apr 14, 1981
Review
12 days
Class
Class II
Product code
CGR
Recalls
None
Predicates
0

1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2004: 1 descendant cleared19801990200020102020
  1. This deviceK810891 Coat-a-Count Cortisol Ria KitDiagnostic Products Corp. · 1981
  2. Descendant · cites it directly · 0 of its ownK042689 Nichols Advantage CortisolNichols Institute Diagnostics · 2004

Most influential descendants

Showing 1 of 1 · See all
  • K042689Nichols Advantage CortisolNichols Institute Diagnostics · 2004 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K810891Coat-a-Count Cortisol Ria KitDiagnostic Products Corp.1981—
+1K042689Nichols Advantage CortisolNichols Institute Diagnostics2004—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200410
FIG. 1 — Lineage of K810891, 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), 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?

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

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K042689Nichols Advantage CortisolNichols Institute Diagnostics20040

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, K042689 (Nichols Institute Diagnostics, 2004) has gone furthest, with 0 descendants of its own.

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—
Cite this page

510(k) Report. “K810891: Coat-a-Count Cortisol Ria Kit.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K810891

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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