Radial Immuno-Diffusion Plates Iga, Igd, Igg & Igm

FDA 510(k) K851284 · Cooper Biomedical, Inc.

Substantially Equivalent

510(k) numberK851284

Submission

Device name
Radial Immuno-Diffusion Plates Iga, Igd, Igg & Igm
Applicant
Cooper Biomedical, Inc.
Malvern, PA, US
Received
April 1, 1985
Decision date
June 11, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CZP – Iga, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5510
Specialty
Immunology

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K040435Roche Diagnostics Tina-Quant Iga GEN.2CZP · Special Roche Diagnostics Corp.03/10/2004SE
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K993927Wako Iga Ii-Ha, Immunoglobulin Calibrator Set, Immunoglobulin StandradCZP · Traditional Wako Chemicals USA, Inc.01/14/2000SE
K983359IgaCZP · Traditional Abbott Laboratories11/04/1998SE
K962200Quantex IgaCZP · Traditional Instrumentation Laboratory CO09/25/1996SE
K955794Iga Immunoturbidimetric & CalibratorCZP · Traditional Randox Laboratories, Ltd.04/05/1996SE
K955907Boehringer Mannheim Iga AssayCZP · Traditional Boehringer Mannheim Corp.02/09/1996SE
K952309N Latex IgaCZP · Traditional Behring Diagnostics, Inc.06/20/1995SE

More from Behring Diagnostics, Inc.

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K863301Demand Total ProteinCEK · Traditional 09/26/1986SE
K861926Worthington HDL Precipitating Reagent SetLBR · Traditional 06/27/1986SE
K854130Demand Ethyl AlcoholDIC · Traditional 11/05/1985SE
K853949Demand Acid Phosphatase ReagentCKB · Traditional 10/16/1985SE
K852262Assist Clinical Chemistry AnalyzerJJE · Traditional 06/25/1985SE
K851285Radial Immunodiffusion Plates CSF Igg & CSF AlbumiDCF · Traditional 06/17/1985SE
K851286Radial Immunodiffusion Plates C3 & C4CZW · Traditional 06/05/1985SE
K851287Radial Immunodiffusion Plates TransferrinDDG · Traditional 05/24/1985SE

Questions and answers

When was Radial Immuno-Diffusion Plates Iga, Igd, Igg & Igm cleared by the FDA?

Radial Immuno-Diffusion Plates Iga, Igd, Igg & Igm (K851284) received a 510(k) decision of Substantially Equivalent on June 11, 1985, 71 days after the submission was received.

What is the product code of K851284?

The FDA product code is CZP – Iga, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5510.