510(k) · Cleared
ClearedImmunoglobulin a Test System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dade Behring, Inc. · CFQ Radioimmunoassay, Immunoglobulins (G, A, M)
Cleared on Mar 25, 1999 as substantially equivalent to K922273 (Beckman Instruments, Inc., 1992) after a 31-day review. Its family tree reaches back 1 generation to 1992.
- Decided
- Mar 25, 1999
- Review
- 31 days
- Class
- Class II
- Product code
- CFQ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K922273 (1992). No later device cites it as a predicate yet.
- Root · 1 generation backK922273 Array (R) 360Beckman Instruments, Inc. · 1992
- This deviceK990552 Immunoglobulin a Test SystemDade Behring, Inc. · 1999
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K922273 | Array (R) 360 | Beckman Instruments, Inc. | 1992 | — |
| 0 (this device) | K990552 | Immunoglobulin a Test System | Dade Behring, Inc. | 1999 | — |
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 CFQ? 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 |
|---|---|---|---|
| * | K922273 | Array (R) 360Summary page 1…16, 1999 Name of Product: IGA Flex™ Reagent Cartridge FDA Classification Name: Immunoglobulin A Test System Predicate Device: Beckman Array® Immunoglobulin A Method (K922273) Device Description: The IGA Flex™ reagent cartridge for the Dimension® clinical chemistry system is a quantitative, turbidimetri… | 1992 |
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.
- 7 other devices also cite its predicate K922273.
How does its category compare?
All CFQ devicesCFQ Radioimmunoassay, Immunoglobulins (G, A, M): FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · CFQ
FDA has decided no CFQ device since 2007.
Median 510(k) review, days · CFQ
Too few CFQ 510(k)s in any year since 2007 to give a median.
Recalls per year · CFQ
No recall names CFQ since 2007.
Adverse event reports per year · CFQ
1in 2018
MAUDE reports naming product code CFQ, not matched to any one device; reports are not rates.
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 | 1 |
| 2009 | 0 | — | 0 | 1 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 3 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 1 |
| 2017 | 0 | — | 0 | 0 |
| 2018 | 0 | — | 0 | 1 |
| 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 IGA Flex™ reagent cartridge for the Dimension® Clinical Chemistry System is an in vitro diagnostic device intended to quantitatively measure immunoglobulin A in serum and plasma.
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/K990552 · printed Nov 6, 2026
Cite this page
510(k) Report. “K990552: Immunoglobulin a Test System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K990552
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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