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FDA 510(k)

ABBOTT A-GENT LIQUID MAGNESIUM REAGENT

K-Number: K872311 · 1987-07-09

ApplicantAbbott Laboratories
Decision Date1987-07-09
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ABBOTT A-GENT LIQUID MAGNESIUM REAGENT is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 1987-07-09 under 510(k) number K872311. 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 ABBOTT A-GENT LIQUID MAGNESIUM REAGENT?

ABBOTT A-GENT LIQUID MAGNESIUM REAGENT is a medical device that received FDA 510(k) clearance on 1987-07-09. The listed applicant is Abbott Laboratories. The 510(k) number is K872311.

When did ABBOTT A-GENT LIQUID MAGNESIUM REAGENT receive FDA 510(k) clearance?

ABBOTT A-GENT LIQUID MAGNESIUM REAGENT received FDA 510(k) clearance on 1987-07-09, under 510(k) number K872311.

Who is the listed applicant for ABBOTT A-GENT LIQUID MAGNESIUM REAGENT?

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 ABBOTT A-GENT LIQUID MAGNESIUM REAGENT?

The FDA product code for ABBOTT A-GENT LIQUID MAGNESIUM REAGENT 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.

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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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