BC-3200 Auto Hematology ANALYZER,M-30D Diluent, M-30R Rinse, M-30CFL Lyse, M-30E-Z Cleanser, M-30PROBE Cleanser, BC-3D C

FDA 510(k) K093394 · Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Substantially Equivalent

510(k) numberK093394

Submission

Device name
BC-3200 Auto Hematology ANALYZER,M-30D Diluent, M-30R Rinse, M-30CFL Lyse, M-30E-Z Cleanser, M-30PROBE Cleanser, BC-3D C
Applicant
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Great Neck, NY, US
Received
October 30, 2009
Decision date
April 8, 2010
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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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
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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

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Questions and answers

When was BC-3200 Auto Hematology ANALYZER,M-30D Diluent, M-30R Rinse, M-30CFL Lyse, M-30E-Z Cleanser, M-30PROBE Cleanser, BC-3D C cleared by the FDA?

BC-3200 Auto Hematology ANALYZER,M-30D Diluent, M-30R Rinse, M-30CFL Lyse, M-30E-Z Cleanser, M-30PROBE Cleanser, BC-3D C (K093394) received a 510(k) decision of Substantially Equivalent on April 8, 2010, 160 days after the submission was received.

What is the product code of K093394?

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