510(k) · Cleared
Recalled · 2009Cell-Dyn 1200 System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Abbott Laboratories · GKZ Counter, Differential Cell
Cleared on Jun 23, 1999 as substantially equivalent to K870233 (Abbott Diagnostics, 1987) after a 79-day review. Its family tree reaches back 1 generation to 1987. It has been recalled once.
- Decided
- Jun 23, 1999
- Review
- 79 days
- Class
- Class II
- Product code
- GKZ
- Recalls
- 1
- Predicates
- 1
Its longest line of descent runs back 1 generation to K870233 (1987). No later device cites it as a predicate yet.
- Root · 1 generation backK870233 Cell-Dyn 1600 Multiparameter Auto. Hema. AnalyzerAbbott Diagnostics · 1987 · Recalled
- This deviceK991142 Cell-Dyn 1200 SystemAbbott Laboratories · 1999
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K870233 | Cell-Dyn 1600 Multiparameter Auto. Hema. Analyzer | Abbott Diagnostics | 1987 | 5 |
| 0 (this device) | K991142 | Cell-Dyn 1200 System | Abbott Laboratories | 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 GKZ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new GKZ device
- #1 K250943 Sysmex XR-Series (XR-10) Automated Hematology…score 13.2 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K870233 | Cell-Dyn 1600 Multiparameter Auto. Hema. AnalyzerSummary page 1…00 System Common Name: Automated Hematology Analyzer Classification Name: Automated Differential Cell Counter 21 CFR 864.5220 Predicate Devices: CELL-DYN® 1700 System, K870233 Manual Differential Description of Device: The CELL-DYN® 1200 System is a single unit device with a stand alone printer used in… | 1987 |
| * | — | Manual Differential Named without a submission number |
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 |
|---|---|---|---|---|
| Nov 30, 2009 | Not classified | Z-1698-2011 | Other | The use of the device assemblies has been extended to a 6 month useful life. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Its one ancestor has a recall.
- 1 other device also cites its predicate K870233.
How does its category compare?
All GKZ devicesGKZ Counter, Differential Cell: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · GKZ
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · GKZ
108in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · GKZ
1in 2025
Class I (2 since 2007) Class II/III not classified
Adverse event reports per year · GKZ
77in 2025
MAUDE reports naming product code GKZ, 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 | 6 | 117 | 37 | 268 |
| 2008 | 6 | 99 | 5 | 925 |
| 2009 | 6 | 147 | 13 | 559 |
| 2010 | 4 | 290 | 27 | 896 |
| 2011 | 3 | 315 | 28 | 2,905 |
| 2012 | 3 | 408 | 7 | 2,959 |
| 2013 | 1 | — | 6 | 3,070 |
| 2014 | 3 | 165 | 0 | 3,112 |
| 2015 | 3 | 273 | 3 | 1,972 |
| 2016 | 3 | 198 | 3 | 3,338 |
| 2017 | 4 | 280 | 3 | 229 |
| 2018 | 3 | 270 | 2 (2) | 497 |
| 2019 | 5 | 210 | 2 | 908 |
| 2020 | 1 | — | 1 | 342 |
| 2021 | 0 | — | 0 | 391 |
| 2022 | 3 | 638 | 4 | 198 |
| 2023 | 4 | 329 | 1 | 155 |
| 2024 | 3 | 157 | 0 | 115 |
| 2025 | 4 | 108 | 1 | 77 |
| 2026 | 4 | 254 | 0 | — |
What is it indicated for?
The CELL-DYN® 1200 is a multi-parameter hematology analyzer intended to classify the following formed elements of EDTA anti-coagulated blood: White Blood Cell Parameters: Red Blood Cell Parameters: WBC — White Blood Cell or leukocyte count RBC -- Red Blood Cell or erythrocyte count GRAN —Granulocyte absolute count HCT — Hematocrit %GRAN -- Granulocyte percent MCYV -- Mean Corpuscular Volume LYM - Lymphocyte absolute count RDW -- Red Cell Distribution…
Read the full statement (137 words)
The CELL-DYN® 1200 is a multi-parameter hematology analyzer intended to classify the following formed elements of EDTA anti-coagulated blood:
White Blood Cell Parameters: Red Blood Cell Parameters:
WBC — White Blood Cell or leukocyte count RBC -- Red Blood Cell or erythrocyte count
GRAN —Granulocyte absolute count HCT — Hematocrit
%GRAN -- Granulocyte percent MCYV -- Mean Corpuscular Volume
LYM - Lymphocyte absolute count RDW -- Red Cell Distribution Width
%L — Lymphocyte percent
MID — Mid-range absolute count Hemoglobin Parameters:
%M — Mid-range percent HGB - Hemoglobin concentration
Platelet Parameters: MCH -- Mean Cell Hemoglobin
PLT — Platelet Count MCHC - Mean Cell Hemoglobin Concentration
MPYV — Mean Platelet Volume
*PDW — Platelet Distribution Width
*PCT — Plateletcrit
* Clinical significance has not been established for these parameters. Therefore, they are not reportable in the US
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/K991142 · printed Nov 6, 2026
Cite this page
510(k) Report. “K991142: Cell-Dyn 1200 System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K991142
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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