Gil Chem Magnesium Reagent

FDA 510(k) K820976 · Gilford Diagnostics

Substantially Equivalent

510(k) numberK820976

Submission

Device name
Gil Chem Magnesium Reagent
Applicant
Gilford Diagnostics
Mchenry, IL, US
Received
April 6, 1982
Decision date
April 26, 1982
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
JGJ – Photometric Method, Magnesium
Device class
Class I (low risk)
Regulation
21 CFR 862.1495
Specialty
Clinical Chemistry

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K162399Atellica CH Magnesium (Mg)JGJ · Traditional Siemens Healthcare Diagnostics, Inc.01/19/2017SE
K122302Ace Magnesium RegentJGJ · Special Alfa Wassermann Diagnostics Technologies, LLC08/27/2012SE
K111915Magnesium AssayJGJ · Traditional Sekisui Diagnostics P.E.I., Inc.12/02/2011SE
K092737Easyra MG Reagent, Model 10220JGJ · Special Medica Corp.11/17/2009SE
K091910Piccolo Magnesium Test SystemJGJ · Special Abaxis, Inc.10/01/2009SE
K063208Magnesium Assay (XB), Models 125-12, 125-50 and 125-S7JGJ · Traditional Diagnostic Chemicals , Ltd.01/19/2007SE
K040508Vitalab Magnesium ReagentJGJ · Traditional Clinical Data, Inc.03/08/2004SE

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Questions and answers

When was Gil Chem Magnesium Reagent cleared by the FDA?

Gil Chem Magnesium Reagent (K820976) received a 510(k) decision of Substantially Equivalent on April 26, 1982, 20 days after the submission was received.

What is the product code of K820976?

The FDA product code is JGJ – Photometric Method, Magnesium, a Class I (low risk) device regulated under 21 CFR 862.1495.