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FDA 510(k)

MEGNESIUM REAGENT KIT

K-Number: K821102 · 1982-05-05

Decision Date1982-05-05
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MEGNESIUM REAGENT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Anco Medical Reagents & Assoc.. It received FDA 510(k) clearance on 1982-05-05 under 510(k) number K821102. 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 MEGNESIUM REAGENT KIT?

MEGNESIUM REAGENT KIT is a medical device that received FDA 510(k) clearance on 1982-05-05. The listed applicant is Anco Medical Reagents & Assoc.. The 510(k) number is K821102.

When did MEGNESIUM REAGENT KIT receive FDA 510(k) clearance?

MEGNESIUM REAGENT KIT received FDA 510(k) clearance on 1982-05-05, under 510(k) number K821102.

Who is the listed applicant for MEGNESIUM REAGENT KIT?

The FDA 510(k) record lists Anco Medical Reagents & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEGNESIUM REAGENT KIT?

The FDA product code for MEGNESIUM REAGENT KIT is JGJ.

Related Clinical Trials

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.

Other records listing Anco Medical Reagents & Assoc. as applicant

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.

View all 26 devices →

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.

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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