Multichem (R) Magnesium Reagent

FDA 510(k) K874595 · Simmler, Inc.

Substantially Equivalent

510(k) numberK874595

Submission

Device name
Multichem (R) Magnesium Reagent
Applicant
Simmler, Inc.
St. Louis, MO, US
Received
November 9, 1987
Decision date
January 21, 1988
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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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

More from Clinical Data, Inc.

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K874820Multichem HDL Precipitating Reagent #S0914LBR · Traditional 01/07/1988SE
K874812Multichem Chloride Reagent S0933CHJ · Traditional 12/18/1987SE
K874311Multichem (R) Total BilirubinCIG · Traditional 11/25/1987SE
K874049Multichem Albumin Reagent S0902CIX · Traditional 10/29/1987SE
K874038Multichem Inorganic Phosphorous S0923CEO · Traditional 10/28/1987SE
K873725Multichem Creatinine Reagent S0917CGX · Traditional 10/20/1987SE
K873761Multichem Alkaline Phosphatase (S0903)CJE · Traditional 10/07/1987SE
K873697Multichem Calcium S0910CIC · Traditional 10/02/1987SE

Questions and answers

When was Multichem (R) Magnesium Reagent cleared by the FDA?

Multichem (R) Magnesium Reagent (K874595) received a 510(k) decision of Substantially Equivalent on January 21, 1988, 73 days after the submission was received.

What is the product code of K874595?

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