Radial Immunodiffusion Plates CSF Igg & CSF Albumi

FDA 510(k) K851285 · Cooper Biomedical, Inc.

Substantially Equivalent

510(k) numberK851285

Submission

Device name
Radial Immunodiffusion Plates CSF Igg & CSF Albumi
Applicant
Cooper Biomedical, Inc.
Malvern, PA, US
Received
April 1, 1985
Decision date
June 17, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DCF – Albumin, Antigen, Antiserum, Control
Device class
Class II (moderate risk)
Regulation
21 CFR 866.5040
Specialty
Immunology

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K852262Assist Clinical Chemistry AnalyzerJJE · Traditional 06/25/1985SE
K851284Radial Immuno-Diffusion Plates Iga, Igd, Igg & IgmCZP · Traditional 06/11/1985SE
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Questions and answers

When was Radial Immunodiffusion Plates CSF Igg & CSF Albumi cleared by the FDA?

Radial Immunodiffusion Plates CSF Igg & CSF Albumi (K851285) received a 510(k) decision of Substantially Equivalent on June 17, 1985, 77 days after the submission was received.

What is the product code of K851285?

The FDA product code is DCF – Albumin, Antigen, Antiserum, Control, a Class II (moderate risk) device regulated under 21 CFR 866.5040.