510(k) · Cleared
Recalled · Class II · 2024Randox Microalbumin
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Randox Laboratories, Ltd. · DDZ Albumin, Fitc, Antigen, Antiserum, Control
Cleared on Oct 5, 2000 after a 38-day review. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known. 1 later device descends from it. It has been recalled once.
- Decided
- Oct 5, 2000
- Review
- 38 days
- Class
- Class II
- Product code
- DDZ
- Recalls
- 1
- Predicates
- 0
1 later device descends from it, 1 citing it directly.
- This deviceK002674 Randox MicroalbuminRandox Laboratories, Ltd. · 2000
- Descendant · cites it directly · 0 of its ownK050576 Microalbumin Tia Reagent; Malb Calibrator Set 200; Malb Control-L…Good Biotech Corp. · 2005
Most influential descendants
Showing 1 of 1 · See all- K050576Microalbumin Tia Reagent; Malb Calibrator Set 200; Malb Control-L, Control-HGood Biotech Corp. · 2005 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K002674 | Randox Microalbumin | Randox Laboratories, Ltd. | 2000 | — |
| +1 | K050576 | Microalbumin Tia Reagent; Malb Calibrator Set 200; Malb Control-L, Control-H | Good Biotech Corp. | 2005 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
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 DDZ? 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?
FDA lists a 510(k) statement for it but has not posted the file, 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.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K050576 | Microalbumin Tia Reagent; Malb Calibrator Set 200; Malb Control-L, Control-H | 2005 | 0 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Jan 31, 2024 | Class II | Z-1594-2024 | Under Investigation by firm | Microalbumin Calibrator Series, MA1567 & MA2426, is running with a negative bias compared to other method may misclassify patient results. Users may experience a shift in Quality Control and patient sample recovery of up to +12%. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K050576 (Good Biotech Corp., 2005) has gone furthest, with 0 descendants of its own.
How does its category compare?
All DDZ devicesDDZ Albumin, Fitc, Antigen, Antiserum, Control: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · DDZ
FDA has decided no DDZ device since 2007.
Median 510(k) review, days · DDZ
Too few DDZ 510(k)s in any year since 2007 to give a median.
Recalls per year · DDZ
No recall names DDZ since 2007.
Adverse event reports per year · DDZ
No MAUDE report names DDZ 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 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 0 |
| 2017 | 0 | — | 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 | — |
https://510kreport.com/device/K002674 · printed Nov 5, 2026
Cite this page
510(k) Report. “K002674: Randox Microalbumin.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K002674
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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