510(k) · Cleared
Recalled · 2010Access Estradiol Reagents on the Access Immunoassay Analyzer
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Beckman Instruments, Inc. · CHP Radioimmunoassay, Estradiol
Cleared on Oct 31, 1997 after a 30-day review. The FDA summary names its predicate without a number. 1 later device descends from it. It has been recalled 2 times.
- Decided
- Oct 31, 1997
- Review
- 30 days
- Class
- Class I
- Product code
- CHP
- Recalls
- 2
- Predicates
- 0
1 later device descends from it, 1 citing it directly.
- This deviceK973743 Access Estradiol Reagents on the Access Immunoassay AnalyzerBeckman Instruments, Inc. · 1997
- Descendant · cites it directly · 0 of its ownK080166 Access Estradiol Calibrators on the Access Immunoassay Systems…Beckman Coulter, Inc. · 2008
Most influential descendants
Showing 1 of 1 · See all- K080166Access Estradiol Calibrators on the Access Immunoassay Systems, Model 33545Beckman Coulter, Inc. · 2008 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K973743 | Access Estradiol Reagents on the Access Immunoassay Analyzer | Beckman Instruments, Inc. | 1997 | — |
| +1 | K080166 | Access Estradiol Calibrators on the Access Immunoassay Systems, Model 33545 | Beckman Coulter, Inc. | 2008 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2008 | 1 | 0 |
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 CHP? 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 |
|---|---|---|---|
| * | — | Abbott IMx® Estradiot Kit Named without a submission number |
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 |
|---|---|---|---|
| K080166 | Access Estradiol Calibrators on the Access Immunoassay Systems, Model 33545 | 2008 | 0 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Mar 4, 2010 | Not classified | Z-0448-2011 | Other | The recall was initiated after Beckman Coulter confirmed that three lots of Access Estradiol reagent (REF 33540) contains an incorrect raw material which may produce incorrect patient results. |
| May 8, 2003 | Not classified | Z-0872-03 | Other | Short volume, resulting possibility of falsely elevated results. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K080166 (Beckman Coulter, Inc., 2008) has gone furthest, with 0 descendants of its own.
How does its category compare?
All CHP devicesCHP Radioimmunoassay, Estradiol: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · CHP
FDA has decided no CHP device since 2007.
Median 510(k) review, days · CHP
Too few CHP 510(k)s in any year since 2007 to give a median.
Recalls per year · CHP
7in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · CHP
84in 2025
MAUDE reports naming product code CHP, 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 | — | 1 | 0 |
| 2008 | 0 | — | 0 | 1 |
| 2009 | 0 | — | 0 | 9 |
| 2010 | 0 | — | 1 | 12 |
| 2011 | 0 | — | 0 | 10 |
| 2012 | 0 | — | 0 | 15 |
| 2013 | 0 | — | 0 | 4 |
| 2014 | 0 | — | 0 | 12 |
| 2015 | 0 | — | 0 | 18 |
| 2016 | 0 | — | 1 | 29 |
| 2017 | 0 | — | 1 | 39 |
| 2018 | 0 | — | 1 | 38 |
| 2019 | 0 | — | 0 | 36 |
| 2020 | 0 | — | 0 | 135 |
| 2021 | 0 | — | 1 | 43 |
| 2022 | 0 | — | 7 | 61 |
| 2023 | 0 | — | 0 | 60 |
| 2024 | 0 | — | 0 | 65 |
| 2025 | 0 | — | 0 | 84 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Access Estradiol assay is a paramagnetic particle, chemiluminescent immunoassay for the
quantitative determination of estradiol levels in human serum, using the Access Immunoassay
System.
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/K973743 · printed Nov 4, 2026
Cite this page
510(k) Report. “K973743: Access Estradiol Reagents on the Access Immunoassay Analyzer.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K973743
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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