Cellsoft(Tm)-Casa (Series 1000,2000 & 3000)

FDA 510(k) K872145 · Cryo Corp.

Substantially Equivalent

510(k) numberK872145

Submission

Device name
Cellsoft(Tm)-Casa (Series 1000,2000 & 3000)
Applicant
Cryo Corp.
Washington, DC, US
Received
June 4, 1987
Decision date
November 13, 1987
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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K001683Sysmex R-500GKL · Traditional Sysmex Corporation of America08/21/2000SE
K991070Coulter Z2 AnalyzerGKL · Traditional Coulter Corp.05/11/1999SE
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Questions and answers

When was Cellsoft(Tm)-Casa (Series 1000,2000 & 3000) cleared by the FDA?

Cellsoft(Tm)-Casa (Series 1000,2000 & 3000) (K872145) received a 510(k) decision of Substantially Equivalent on November 13, 1987, 162 days after the submission was received.

What is the product code of K872145?

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