Multistat III Magnesium Test

FDA 510(k) K771469 · Instrumentation Laboratory CO

Substantially Equivalent

510(k) numberK771469

Submission

Device name
Multistat III Magnesium Test
Applicant
Instrumentation Laboratory CO
Mchenry, IL, US
Received
August 4, 1977
Decision date
September 12, 1977
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

Other 510(k)s with product code JGJ

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K181748MagnesiumJGJ · Traditional Abbott Laboratories09/12/2018SE
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K162200Randox RX Daytona Plus Magnesium (MG)JGJ · Traditional Randox Laboratories, Ltd.04/28/2017SE
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 Multistat III Magnesium Test cleared by the FDA?

Multistat III Magnesium Test (K771469) received a 510(k) decision of Substantially Equivalent on September 12, 1977, 39 days after the submission was received.

What is the product code of K771469?

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