Atac 4300 Hematology Cell Counter

FDA 510(k) K863332 · Turpen Laboratory Systems, Inc.

Substantially Equivalent

510(k) numberK863332

Submission

Device name
Atac 4300 Hematology Cell Counter
Applicant
Turpen Laboratory Systems, Inc.
Lakewood, NJ, US
Received
August 27, 1986
Decision date
September 29, 1986
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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K152776Glocyte Automated Cell Counter SystemGKL · Traditional Advanced Instruments, Inc.05/27/2016SE
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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

More from Sysmex Corp.

510(k)DeviceDecision
K870836Atac 1500 Chemistry AnalyzerJJE · Traditional 04/01/1987SE
K851321Atac 2000 Chemistry AnalyzerJQP · Traditional 04/25/1985SE
K843059Atac 2000JJE · Traditional 10/11/1984SE
K832115Atac 3000JJE · Traditional 01/10/1984SE
K832116Atac 4700 Hematology Cell CounterGIF · Traditional 10/20/1983SE

Questions and answers

When was Atac 4300 Hematology Cell Counter cleared by the FDA?

Atac 4300 Hematology Cell Counter (K863332) received a 510(k) decision of Substantially Equivalent on September 29, 1986, 33 days after the submission was received.

What is the product code of K863332?

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