Cell-Dyn 3000 Multi-Parameter Hematology Analyer

FDA 510(k) K890491 · Abbott Diagnostics

Substantially Equivalent

510(k) numberK890491

Submission

Device name
Cell-Dyn 3000 Multi-Parameter Hematology Analyer
Applicant
Abbott Diagnostics
Mountain View, CA, US
Received
January 31, 1989
Decision date
April 18, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKZ – Counter, Differential Cell
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5220
Specialty
Hematology

Other 510(k)s with product code GKZ

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K243348Athelas HomeGKZ · Traditional Athelas, Inc.02/06/2026SE
K251249Tru Hematology TestGKZ · Traditional Truvian Sciences, Inc.01/16/2026SE
K251371Sysmex XR-Series (XR-20) Automated Hematology AnalyzerGKZ · Traditional Sysmex America, Inc.06/25/2025SE
K250943Sysmex XR-Series (XR-10) Automated Hematology AnalyzerGKZ · Traditional Sysmex America, Inc.06/25/2025SE
K243283Alinity h-series SystemGKZ · Traditional Abbott Laboratories02/20/2025SE
K240402Cito CBC SystemGKZ · Dual Track Cytochip, Inc.02/03/2025SE
K240252UniCel DxH 900 Coulter Cellular Analysis System; UniCel DxH Slidemaker Stainer II…GKZ · Traditional Beckman Coulter, Inc.07/05/2024SE
K232946Yumizen H2500GKZ · Traditional Horiba Abx SAS05/21/2024SE
K240636HemoScreen Hematology AnalyzerGKZ · Abbreviated Pixcell Medical Technologies05/02/2024SE

More from Pixcell Medical Technologies

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K964185Imx Ca 125LTK · Traditional 11/04/1997SE
K972182Abbott Strep a ControlsMJZ · Traditional 08/13/1997SE
K961439Abbott Cell-Dyn 4000 SystemGKZ · Traditional 10/18/1996SE
K881242Cell-Dyn Rapid-Lyse and HemogloblinGJZ · Traditional 04/21/1988SE
K881130Cell-Dyn Isotonic DiluentGIF · Traditional 03/31/1988SE
K873348Cell-Dyn Diff Screen, Auto. & Semi Auto. Lytic Ag.GGK · Traditional 09/09/1987SE
K873347Cell-Dyn Diff. Screen Isotonic DiluentGIF · Traditional 09/09/1987SE
K873408Model 690 SpectrophotometerJJQ · Traditional 09/08/1987SE
K872761Cell-Dyn 610 Hematology AnalyzerGKZ · Traditional 08/06/1987SE
K870233Cell-Dyn 1600 Multiparameter Auto. Hema. AnalyzerGKZ · Traditional 03/17/1987SE

Questions and answers

When was Cell-Dyn 3000 Multi-Parameter Hematology Analyer cleared by the FDA?

Cell-Dyn 3000 Multi-Parameter Hematology Analyer (K890491) received a 510(k) decision of Substantially Equivalent on April 18, 1989, 77 days after the submission was received.

What is the product code of K890491?

The FDA product code is GKZ – Counter, Differential Cell, a Class II (moderate risk) device regulated under 21 CFR 864.5220.