510(k) · Cleared
Recalled · 2006Kodak Ektachem Clinical Chemistry Slides
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Eastman Kodak Company · CHI Lipase-Esterase, Enzymatic, Photometric, Lipase
Cleared on Jan 18, 1985 after a 22-day review. FDA has not posted a summary or statement for it, so its predicates are not known. It has been recalled once.
- Decided
- Jan 18, 1985
- Review
- 22 days
- Class
- Class I
- Product code
- CHI
- Recalls
- 1
- Predicates
- 0
FDA has not posted a summary or statement for it, so its predicates are not known.
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 CHI? 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 has not posted a summary or statement for it, so its predicates are not known.
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Oct 9, 2006 | Not classified | Z-0245-2007 | Other | The firm identified circumstances in which biased results or calibration failures can be observed when using any lot of VITROS LIPA slides if they have been stored on the VITROS Chemistry Systems for more than 2 days. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All CHI devicesCHI Lipase-Esterase, Enzymatic, Photometric, Lipase: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · CHI
FDA has decided no CHI device since 2007.
Median 510(k) review, days · CHI
Too few CHI 510(k)s in any year since 2007 to give a median.
Recalls per year · CHI
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · CHI
11in 2025
MAUDE reports naming product code CHI, 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 | — | 4 | 1 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 1 | 2 |
| 2011 | 0 | — | 0 | 4 |
| 2012 | 0 | — | 0 | 1 |
| 2013 | 0 | — | 1 | 0 |
| 2014 | 0 | — | 1 | 1 |
| 2015 | 0 | — | 0 | 5 |
| 2016 | 0 | — | 0 | 3 |
| 2017 | 0 | — | 0 | 4 |
| 2018 | 0 | — | 3 | 6 |
| 2019 | 0 | — | 0 | 2 |
| 2020 | 0 | — | 0 | 32 |
| 2021 | 0 | — | 0 | 2 |
| 2022 | 0 | — | 0 | 4 |
| 2023 | 0 | — | 1 | 4 |
| 2024 | 0 | — | 0 | 6 |
| 2025 | 0 | — | 0 | 11 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K845027 · printed Nov 4, 2026
Cite this page
510(k) Report. “K845027: Kodak Ektachem Clinical Chemistry Slides.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K845027
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Record history
- FDA decision record loaded May 2, 2026
- Page last updated Nov 3, 2026