510(k) Report

510(k) · Cleared

Cleared

CHOL

K981652510(k) TraditionalCleared Jun 29, 199849-day reviewClass I21 CFR 862.1175

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

Abbott Laboratories · CHH Enzymatic Esterase--Oxidase, Cholesterol

Cleared on Jun 29, 1998 as substantially equivalent to K854298 (Boehringer Mannheim Corp., 1985) after a 49-day review. Its family tree reaches back 1 generation to 1985. 1 later device descends from it.

Decided
Jun 29, 1998
Review
49 days
Class
Class I
Product code
CHH
Recalls
None
Predicates
1

Its longest line of descent runs back 1 generation to K854298 (1985). 1 later device descends from it, 1 citing it directly.

Descendants, by year cleared 2022: 1 descendant clearedK854298 · IRON · Boehringer Mannheim Corp. · 19851990200020102020
Descendants, by generation 1 generation forward: 1 descendant K854298 · IRON · Boehringer Mannheim Corp. · 19850
  1. Root · 1 generation backK854298 IRONBoehringer Mannheim Corp. · 1985
  2. This deviceK981652 CHOLAbbott Laboratories · 1998
  3. Descendant · cites it directly · 0 of its ownK203597 Cholesterol2Abbott Ireland Diagnostics Division · 2022

Most influential descendants

Showing 1 of 1 · See all
  • K203597Cholesterol2Abbott Ireland Diagnostics Division · 2022 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−1K854298IRONBoehringer Mannheim Corp.1985—
0 (this device)K981652CHOLAbbott Laboratories1998—
+1K203597Cholesterol2Abbott Ireland Diagnostics Division2022—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202210
FIG. 1 — Lineage of K981652, 1985–2022Source: 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 CHH? 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 CHH device

  1. #1 K251091 Lipidsscore 10.9 · 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
*K854298IRON
Summary page 3
…1 Substantial Equivalence: The Cholesterol assay is substantially equivalent to the Boehringer Mannheim® Cholesterol assay on the Hitachi® 717 Analyzer (K854298). These assays yield similar Performance Characteristics. Similarities: « Both assays are in vitro clinical chemistry methods. .…
Boehringer Mannheim Corp.1985—

Also cleared against K854298: 1 other device →

What descends from it? (1)

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

NumberDeviceApplicantDecidedDescendants
K203597Cholesterol2Abbott Ireland Diagnostics Division20220

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.
  • Of its descendants, K203597 (Abbott Ireland Diagnostics Division, 2022) has gone furthest, with 0 descendants of its own.
  • 1 other device also cites its predicate K854298.

How does its category compare?

All CHH devices

CHH Enzymatic Esterase--Oxidase, Cholesterol: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · CHH

1in 2025

2007: 22008: 22009: 12011: 12012: 42013: 12014: 12015: 12016: 12017: 12018: 22019: 12022: 12024: 12025: 1
2007high 4 (2012) · low 0 (2010)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · CHH

198in 2012

2012: 198 days median
2007high 198 (2012)2026

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

Recalls per year · CHH

2in 2021

2009: 32010: 22013: 12014: 12016: 22021: 22026 (partial year): 1
2007high 3 (2009) · low 0 (2007)2026

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

Adverse event reports per year · CHH

14in 2025

2007: 12010: 102011: 182012: 112014: 12016: 52017: 22018: 12019: 52020: 12021: 22022: 42023: 42024: 82025: 14
2007high 18 (2011) · low 0 (2008)2025

MAUDE reports naming product code CHH, 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
20072—01
20082—00
20091—30
20100—210
20111—018
20124198011
20131—10
20141—11
20151—00
20161—25
20171—02
20182—01
20191—05
20200—01
20210—22
20221—04
20230—04
20241—08
20251—014
20260—1—

What is it indicated for?

The Cholesterol assay is used for the quantitation of cholesterol in human serum or plasma. Cholesterol measurements are used in the diagnosis and treatment of disorders involving excess cholesterol in the blood and lipid and lipoprotein metabolism disorders.

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. “K981652: CHOL.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K981652

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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