Erma PC-602 PC-603 Blood Cell Counter

FDA 510(k) K854678 · Future Impex Corp.

Substantially Equivalent

510(k) numberK854678

Submission

Device name
Erma PC-602 PC-603 Blood Cell Counter
Applicant
Future Impex Corp.
Deerpark, NY, US
Received
December 5, 1985
Decision date
February 24, 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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K050235Iq 200 Urine Analyzer Body Fluids ModuleGKL · Traditional Iris International, Inc.03/23/2005SE
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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.

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K861487ST-90 Spiro AnalizerBTY · Traditional 06/23/1986SE
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K854686TE-25 Coaguro MeterJBP · Traditional 06/04/1986SE
K854685DIGITAL-9 Key Leucocyte CounterGKM · Traditional 04/04/1986SE
K854677Erma PC-604 Blood Cell CounterGKL · Traditional 02/24/1986SE
K854679PHOTIC-100 SpectrophotometerJJQ · Traditional 02/20/1986SE
K843934Model {M-102 I-Channel Electro Cardiograph UnitDPS · Traditional 11/20/1984SE
K843984PM-80 PulmotesterBZG · Traditional 10/24/1984SE
K843700ST-200A W/Maximal Voluntary Ventillat- · Traditional 10/24/1984SE
K832433Automatic Spirometer ST-200BZG · Traditional 09/29/1983SE

Questions and answers

When was Erma PC-602 PC-603 Blood Cell Counter cleared by the FDA?

Erma PC-602 PC-603 Blood Cell Counter (K854678) received a 510(k) decision of Substantially Equivalent on February 24, 1986, 81 days after the submission was received.

What is the product code of K854678?

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