D3 Hematology Analyzer, Model D3

FDA 510(k) K071562 · Drew Scientific, Inc.

Substantially Equivalent

510(k) numberK071562

Submission

Device name
D3 Hematology Analyzer, Model D3
Applicant
Drew Scientific, Inc.
Dallas, TX, US
Received
June 7, 2007
Decision date
December 11, 2007
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
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K240636HemoScreen Hematology AnalyzerGKZ · Abbreviated Pixcell Medical Technologies05/02/2024SE

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Questions and answers

When was D3 Hematology Analyzer, Model D3 cleared by the FDA?

D3 Hematology Analyzer, Model D3 (K071562) received a 510(k) decision of Substantially Equivalent on December 11, 2007, 187 days after the submission was received.

What is the product code of K071562?

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