510(k) Report

510(k) · Cleared

Cleared

Immage Immunochemistry System Ferritin (Fer)Reagent, Immage Immunochemistry System Ferritin Calibrator

K983340510(k) TraditionalCleared Dec 14, 199882-day reviewClass II21 CFR 866.5340

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

Beckman Coulter, Inc. · DBF Ferritin, Antigen, Antiserum, Control

Cleared on Dec 14, 1998 after an 82-day review. The summary cites one number, which could not be confirmed as its predicate (see the table below).

Decided
Dec 14, 1998
Review
82 days
Class
Class II
Product code
DBF
Recalls
None
Predicates
1

The summary cites one number, which could not be confirmed as its predicate (see the table below).

FIG. 1 — Lineage of K983340Source: FDA 510(k) database · 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 DBF? 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 DBF device

  1. #1 K193650 LIAISON Ferritinscore 2.0 · 1 generation · no Class I recall
  2. #2 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; numbers the summary cites that cannot be its predicate are marked – and kept off the family tree.

TypeNumberDeviceApplicantDecidedRecalls
Kept off the family treeK941365FDA’s K941365 is Mpi Denture Adhesive Film Seals
Not matched in our reading of the summary (scans can blur digits), so it is kept off the family tree
Medical Polymers, Inc.1994—

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.

How does its category compare?

All DBF devices

DBF Ferritin, Antigen, Antiserum, Control: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · DBF

1in 2021

2009: 12010: 12011: 12012: 12014: 12017: 12020: 12021: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DBF

Too few DBF 510(k)s in any year since 2007 to give a median.

Recalls per year · DBF

3in 2012

2012: 3
2007high 3 (2012) · low 0 (2007)2026

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

Adverse event reports per year · DBF

1in 2025

2012: 12013: 12016: 12017: 22018: 72019: 12020: 12021: 32023: 32024: 12025: 1
2007high 7 (2018) · low 0 (2007)2025

MAUDE reports naming product code DBF, 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
20091—00
20101—00
20111—00
20121—31
20130—01
20141—00
20150—00
20160—01
20171—02
20180—07
20190—01
20201—01
20211—03
20220—00
20230—03
20240—01
20250—01
20260—0—

What is it indicated for?

The IMMAGE® Immunochemistry System Ferritin (FER) Reagent, when used in conjunction with Beckman Coulter IMMAGE® Immunochemistry Systems and Beckman Coulter Ferritin Calibrator, is intended for the quantitative determination of ferritin in human serum by turbidimetric immunoassay.

Beckman Coulter Ferritin Calibrator, when used in conjunction with Ferritin reagent, is intended for use on IMMAGE® Immunochemistry Systems for the calibration of ferritin.

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. “K983340: Immage Immunochemistry System Ferritin (Fer)Reagent, Immage Immunochemistry System Ferritin Calibrator.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K983340

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Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026