Cholesterol Reagent for Demand Analyzer

FDA 510(k) K844242 · Advanced Biomedical Methods, Inc.

Substantially Equivalent

510(k) numberK844242

Submission

Device name
Cholesterol Reagent for Demand Analyzer
Applicant
Advanced Biomedical Methods, Inc.
Niles, IL, US
Received
November 1, 1984
Decision date
January 3, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
CHH – Enzymatic Esterase--Oxidase, Cholesterol
Device class
Class I (low risk)
Regulation
21 CFR 862.1175
Specialty
Clinical Chemistry

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More from Axis-Shield Poc AS

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K945353Clarit(Tm)JKA · Traditional 12/09/1994SE
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K852784Alkaline PhosphataseCJE · Traditional 07/22/1985SE
K852783Sgot/Alt ReagentCIT · Traditional 07/22/1985SE
K852027GGTP Reagent/Serum Iron/Salicylate Demand AnalyzerDKJ · Traditional 05/29/1985SE
K850381Magnesium Reagent for Demand AnalyzerJGJ · Traditional 03/01/1985SE
K850380Inorganic Phosphorous for Demand AnalyzerCEO · Traditional 03/01/1985SE
K850379Direct Bilirubin for Demand AnalyzerCIG · Traditional 03/01/1985SE
K850378LDH Reagent for Demand AnalyzerCFJ · Traditional 03/01/1985SE

Questions and answers

When was Cholesterol Reagent for Demand Analyzer cleared by the FDA?

Cholesterol Reagent for Demand Analyzer (K844242) received a 510(k) decision of Substantially Equivalent on January 3, 1985, 63 days after the submission was received.

What is the product code of K844242?

The FDA product code is CHH – Enzymatic Esterase--Oxidase, Cholesterol, a Class I (low risk) device regulated under 21 CFR 862.1175.