Cellect Labtrak Software

FDA 510(k) K874320 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK874320

Submission

Device name
Cellect Labtrak Software
Applicant
Instrumentation Laboratory CO
Lexington, MA, US
Received
October 21, 1987
Decision date
January 27, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
GKL – Counter, Cell, Automated (Particle Counter)
Device class
Class II (moderate risk)
Regulation
21 CFR 864.5200
Specialty
Hematology

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K071652Hemocue WBC SystemGKL · Traditional Hemocue AB10/25/2007SE
K051693Modification to Bayer Advia 2120 Hematology Analyzer with Autoslide SystemGKL · Traditional Bayer Healthcare, LLC12/07/2005SE
K050235Iq 200 Urine Analyzer Body Fluids ModuleGKL · Traditional Iris International, Inc.03/23/2005SE
K032677Sysmex POCH-100IGKL · Traditional Sysmex America, Inc.02/11/2004SE
K022331Advia 120 Hematology System, Cerebrospinal Fluid MethodGKL · Special Bayer Diagnostics Corp.09/11/2002SE
K001683Sysmex R-500GKL · Traditional Sysmex Corporation of America08/21/2000SE
K991070Coulter Z2 AnalyzerGKL · Traditional Coulter Corp.05/11/1999SE
K981950Sysmex R-3500, Automated Reticculocyte Analyzer, Model R-3500GKL · Traditional Sysmex Corp.11/03/1998SE

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Questions and answers

When was Cellect Labtrak Software cleared by the FDA?

Cellect Labtrak Software (K874320) received a 510(k) decision of Substantially Equivalent on January 27, 1988, 98 days after the submission was received.

What is the product code of K874320?

The FDA product code is GKL – Counter, Cell, Automated (Particle Counter), a Class II (moderate risk) device regulated under 21 CFR 864.5200.