Ortho Immunocount Flow Cytometry System

FDA 510(k) K954570 · Ortho Diagnostic Systems, Inc.

Substantially Equivalent

510(k) numberK954570

Submission

Device name
Ortho Immunocount Flow Cytometry System
Applicant
Ortho Diagnostic Systems, Inc.
Raritan, NJ, US
Received
October 2, 1995
Decision date
April 30, 1996
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

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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More from Pixcell Medical Technologies

510(k)DeviceDecision
K951459Ortho-Mune Okt 4A (CD4) - Monoclonal Antibody (Murine) Fitc ConjugateGKZ · Traditional 07/14/1997SE
K951632Ortho-Mune Ok-Combo Control IGG2A-FITC/IGG2A-PE Monoclonal Antibody (Murine)GKZ · Traditional 03/06/1997SE
K964754Ortho-Mune Okb (CD19)- Monoclonal Antibody (Murine) Phycoerythrine ConjugateGKZ · Traditional 01/22/1997SE
K963902Quantitative Fibrinogen AssayGIS · Traditional 11/29/1996SE
K951100Ortho-Mune Ok-Combo CD3-FITC/CD19-PE (OKT3/OKB19A Monolclonal Antibody (Murine)GKZ · Traditional 05/13/1996SE
K950625Ortho-Mune Ok-Combo CD40FITC/CD8-PE (OKT4A/OKT8) Monoclonal Antibody (Murine)GKZ · Traditional 05/13/1996SE
K950568Ortho-Mune Ok-Combo CD3-FITC/CD4-PE (OKT2/OKT4A) Monoclonal Antibody (Murine)GKZ · Traditional 05/13/1996SE
K950482Ortho-Mune Ok-Comvo CD3-FITC/CD8-PE (Okt 3/OKT8) Monoclonal Antibody (Murine)GKZ · Traditional 05/10/1996SE
K935720Ortho Count Calibration Kit for Ortho Cytoronabsolute Laser Flow Cytometry SystemGKZ · Traditional 05/09/1996SE
K955638Synthafax Aptt ReagentGFO · Traditional 04/23/1996SE

Questions and answers

When was Ortho Immunocount Flow Cytometry System cleared by the FDA?

Ortho Immunocount Flow Cytometry System (K954570) received a 510(k) decision of Substantially Equivalent on April 30, 1996, 211 days after the submission was received.

What is the product code of K954570?

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