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FDA 510(k)

AMERICAN MONITOR MAGNESIUM #'S 1036&4021

K-Number: K802091 · 1980-10-10

ApplicantAmerican Monitor Corp.
Decision Date1980-10-10
Product CodeJGJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMERICAN MONITOR MAGNESIUM #'S 1036&4021 is the device name listed in this FDA 510(k) record. The listed applicant is American Monitor Corp.. It received FDA 510(k) clearance on 1980-10-10 under 510(k) number K802091. 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 AMERICAN MONITOR MAGNESIUM #'S 1036&4021?

AMERICAN MONITOR MAGNESIUM #'S 1036&4021 is a medical device that received FDA 510(k) clearance on 1980-10-10. The listed applicant is American Monitor Corp.. The 510(k) number is K802091.

When did AMERICAN MONITOR MAGNESIUM #'S 1036&4021 receive FDA 510(k) clearance?

AMERICAN MONITOR MAGNESIUM #'S 1036&4021 received FDA 510(k) clearance on 1980-10-10, under 510(k) number K802091.

Who is the listed applicant for AMERICAN MONITOR MAGNESIUM #'S 1036&4021?

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

What is the FDA product code for AMERICAN MONITOR MAGNESIUM #'S 1036&4021?

The FDA product code for AMERICAN MONITOR MAGNESIUM #'S 1036&4021 is JGJ.

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Other records listing American Monitor Corp. 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.

K896000ASPARTATE AMINOTRANFERASE (AST)K895999PHOSPHORUSK896001ALANINE AMINOTRANSFERASE (ALT)K895423ACCESS CHEMISTRY ANALYZERK893137EXCEL (TM) CHEMISTRY ANALYZERK892331ENZYMATIC UREA NITROGEN REAGENT SET

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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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