Coulter STKS Analyzer with CD4 & CD8 Lymphocyte Analysis

FDA 510(k) K961278 · Coulter Corp.

Substantially Equivalent

510(k) numberK961278

Submission

Device name
Coulter STKS Analyzer with CD4 & CD8 Lymphocyte Analysis
Applicant
Coulter Corp.
Miami, FL, US
Received
April 3, 1996
Decision date
July 22, 1996
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

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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

More from Pixcell Medical Technologies

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K993356Coulter Hematology Analyzers with Irf & MRV AnalysesGKZ · Traditional 04/20/2000SE
K991070Coulter Z2 AnalyzerGKL · Traditional 05/11/1999SE
K990327Reticone System for Epics XL Flow Cytometry SystemsGKZ · Traditional 04/26/1999SE
K990172Tetraone System for Epics XL Flow Cytometry Systems with Cyto-Stat Tetrachrome…GKZ · Traditional 04/13/1999SE
K990352Coulter Ac T Diff 2 AnalyzerGKZ · Traditional 04/01/1999SE
K984216Immuno-Trol Control CellsJPK · Traditional 03/16/1999SE
K982167Cyto-Stat Trichrome CD45-FITC/CD19-RD1/CD3-PC5 Monoclonal Antibody Reagent with…GKZ · Traditional 11/09/1998SE
K982166Cyto-Stat Trichrome CD45-FITC/CD56-RD1/CD3-PC5 Monoclonal Antibody Reagent with…GKZ · Traditional 11/05/1998SE
K982172Cyto-Stat CD3-FITC/CD56-RDI Monoclonal Antibody Reagent with Cyto-Stat/Coulter Clone…GKZ · Traditional 09/24/1998SE
K973634Coulter Ac.T Diff AnalyzerGKZ · Traditional 10/29/1997SE

Questions and answers

When was Coulter STKS Analyzer with CD4 & CD8 Lymphocyte Analysis cleared by the FDA?

Coulter STKS Analyzer with CD4 & CD8 Lymphocyte Analysis (K961278) received a 510(k) decision of Substantially Equivalent on July 22, 1996, 110 days after the submission was received.

What is the product code of K961278?

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