510(k) · Cleared
ClearedImmage Immunochemistry System Ceruloplasmin (Cer) Reagent
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Beckman Instruments, Inc. · DDB Ceruloplasmin, Antigen, Antiserum, Control
Cleared on Apr 25, 1997 as substantially equivalent to K791339 (Beckman Instruments, Inc., 1979) after a 149-day review. Its family tree reaches back 1 generation to 1979.
- Decided
- Apr 25, 1997
- Review
- 149 days
- Class
- Class II
- Product code
- DDB
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K791339 (1979). No later device cites it as a predicate yet.
- Root · 1 generation backK791339 Human CeruloplasminBeckman Instruments, Inc. · 1979
- This deviceK964762 Immage Immunochemistry System Ceruloplasmin (Cer) ReagentBeckman Instruments, Inc. · 1997
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K791339 | Human Ceruloplasmin | Beckman Instruments, Inc. | 1979 | — |
| 0 (this device) | K964762 | Immage Immunochemistry System Ceruloplasmin (Cer) Reagent | Beckman Instruments, Inc. | 1997 | — |
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 DDB? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin the report
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K791339 | Human CeruloplasminSummary page 1…plasmin (CER) Reagent 3.2 Classification Name Cerulopiasmin immunological test system (21 CFR § 866.5210) IMMAGE System Beckman Ceruloplasmin | Beckman instruments, | K791339 Ceruloplasmin (CER) Description: The IMMAGE Immunochemistry System CER Reagent in conjunction with Beckman Calibrator 2, is inte… | 1979 |
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.
- 1 other device also cites its predicate K791339.
How does its category compare?
All DDB devicesDDB Ceruloplasmin, Antigen, Antiserum, Control: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DDB
1in 2017
2026 to Oct 25, outlined.
Median 510(k) review, days · DDB
Too few DDB 510(k)s in any year since 2007 to give a median.
Recalls per year · DDB
No recall names DDB since 2007.
Adverse event reports per year · DDB
No MAUDE report names DDB since 2007.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 0 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 1 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 1 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 0 |
| 2019 | 0 | — | 0 | 0 |
| 2020 | 0 | — | 0 | 0 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 0 |
| 2023 | 0 | — | 0 | 0 |
| 2024 | 0 | — | 0 | 0 |
| 2025 | 0 | — | 0 | 0 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The IMMAGE Immunochemistry System Ceruloplasmin (CER) Reagent, when used in conjunction with Beckman IMMAGE™ Immunochemistry Systems and Beckman Calibrator 2, is intended for the quantitative determination of human ceruloplasmin by rate nephelometry.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K964762 · printed Nov 4, 2026
Cite this page
510(k) Report. “K964762: Immage Immunochemistry System Ceruloplasmin (Cer) Reagent.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K964762
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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