Radial Immunodiffusion Plates C3 & C4

FDA 510(k) K851286 · Cooper Biomedical, Inc.

Substantially Equivalent

510(k) numberK851286

Submission

Device name
Radial Immunodiffusion Plates C3 & C4
Applicant
Cooper Biomedical, Inc.
Malvern, PA, US
Received
April 1, 1985
Decision date
June 5, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CZW – Complement C3, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5240
Specialty
Immunology

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More from Randox Laboratories, Ltd.

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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
K851284Radial Immuno-Diffusion Plates Iga, Igd, Igg & IgmCZP · Traditional 06/11/1985SE
K851287Radial Immunodiffusion Plates TransferrinDDG · Traditional 05/24/1985SE

Questions and answers

When was Radial Immunodiffusion Plates C3 & C4 cleared by the FDA?

Radial Immunodiffusion Plates C3 & C4 (K851286) received a 510(k) decision of Substantially Equivalent on June 5, 1985, 65 days after the submission was received.

What is the product code of K851286?

The FDA product code is CZW – Complement C3, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5240.