Demand Ethyl Alcohol

FDA 510(k) K854130 · Cooper Biomedical, Inc.

Substantially Equivalent

510(k) numberK854130

Submission

Device name
Demand Ethyl Alcohol
Applicant
Cooper Biomedical, Inc.
Malvern, PA, US
Received
October 9, 1985
Decision date
November 5, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
DIC – Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method
Device class
Class II (moderate risk)
Regulation
21 CFR 862.3040
Specialty
Clinical Toxicology

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More from Dade Behring, Inc.

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K863301Demand Total ProteinCEK · Traditional 09/26/1986SE
K861926Worthington HDL Precipitating Reagent SetLBR · Traditional 06/27/1986SE
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
K851286Radial Immunodiffusion Plates C3 & C4CZW · Traditional 06/05/1985SE
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Questions and answers

When was Demand Ethyl Alcohol cleared by the FDA?

Demand Ethyl Alcohol (K854130) received a 510(k) decision of Substantially Equivalent on November 5, 1985, 27 days after the submission was received.

What is the product code of K854130?

The FDA product code is DIC – Alcohol Dehydrogenase, Specific Reagent For Ethanol Enzyme Method, a Class II (moderate risk) device regulated under 21 CFR 862.3040.