Cellect Model D, Automated Hemtalogy Analyzer

FDA 510(k) K874763 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK874763

Submission

Device name
Cellect Model D, Automated Hemtalogy Analyzer
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
November 19, 1987
Decision date
February 18, 1988
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

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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

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Questions and answers

When was Cellect Model D, Automated Hemtalogy Analyzer cleared by the FDA?

Cellect Model D, Automated Hemtalogy Analyzer (K874763) received a 510(k) decision of Substantially Equivalent on February 18, 1988, 91 days after the submission was received.

What is the product code of K874763?

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