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FDA 510(k)

MAGNESIUM REAGENT (MAGON SULFONATE)

K-Number: K883972 · 1988-11-10

Decision Date1988-11-10
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MAGNESIUM REAGENT (MAGON SULFONATE) is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1988-11-10 under 510(k) number K883972. 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 REAGENT (MAGON SULFONATE)?

MAGNESIUM REAGENT (MAGON SULFONATE) is a medical device that received FDA 510(k) clearance on 1988-11-10. The listed applicant is Sigma Chemical Co.. The 510(k) number is K883972.

When did MAGNESIUM REAGENT (MAGON SULFONATE) receive FDA 510(k) clearance?

MAGNESIUM REAGENT (MAGON SULFONATE) received FDA 510(k) clearance on 1988-11-10, under 510(k) number K883972.

Who is the listed applicant for MAGNESIUM REAGENT (MAGON SULFONATE)?

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

What is the FDA product code for MAGNESIUM REAGENT (MAGON SULFONATE)?

The FDA product code for MAGNESIUM REAGENT (MAGON SULFONATE) 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 Sigma Chemical Co. 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 231 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

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

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