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FDA 510(k)

Magnesium

K-Number: K173294 · 2018-05-18

ApplicantAbbott Laboratories
Decision Date2018-05-18
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

Magnesium is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2018-05-18 under 510(k) number K173294. The device is classified under product code JGJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Magnesium?

Magnesium is a medical device that received FDA 510(k) clearance on 2018-05-18. The listed applicant is Abbott Laboratories. The 510(k) number is K173294.

When did Magnesium receive FDA 510(k) clearance?

Magnesium received FDA 510(k) clearance on 2018-05-18, under 510(k) number K173294.

Who is the listed applicant for Magnesium?

The FDA 510(k) record lists Abbott Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Magnesium?

The FDA product code for Magnesium is JGJ.

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Related Devices (Code: JGJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K181748MagnesiumAbbott LaboratoriesK162200Randox RX Daytona Plus Magnesium (MG)Randox Laboratories, Ltd.K162399Atellica CH Magnesium (Mg)Siemens Healthcare Diagnostics, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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