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FDA 510(k)

MULTI-GAS ANALYZER (MGA)

K-Number: K893589 · 1989-07-27

ApplicantMarquette Gas Analysis Corp.
Decision Date1989-07-27
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MULTI-GAS ANALYZER (MGA) is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Gas Analysis Corp.. It received FDA 510(k) clearance on 1989-07-27 under 510(k) number K893589. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-GAS ANALYZER (MGA)?

MULTI-GAS ANALYZER (MGA) is a medical device that received FDA 510(k) clearance on 1989-07-27. The listed applicant is Marquette Gas Analysis Corp.. The 510(k) number is K893589.

When did MULTI-GAS ANALYZER (MGA) receive FDA 510(k) clearance?

MULTI-GAS ANALYZER (MGA) received FDA 510(k) clearance on 1989-07-27, under 510(k) number K893589.

Who is the listed applicant for MULTI-GAS ANALYZER (MGA)?

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

What is the FDA product code for MULTI-GAS ANALYZER (MGA)?

The FDA product code for MULTI-GAS ANALYZER (MGA) is CCK.

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.

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Other records listing Marquette Gas Analysis 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.

K904863MGA-IR SIDESTREAM PCO2 MODULE

Related Devices (Code: CCK)

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.

K251641GF-310R Multigas Unit (GF-310R)Nihon Kohden CorporationK261633VisuBreathAffirm Medical Technologies II, LLCK253030Capnostream™35 Portable Respiratory Monitor (PM35MN)Covidien, LLCK250148Medical Gas Analyzer (AG200)Prior Care Science Technology, Ltd.K243956TG-980P CO2 Sensor Kit (TG-980P); TG-980P1 CO2 Sensor Kit (TG-980P1)Nihon Kohden CorporationK2512160184 CO2 Sampling line; 0184T CO2 Sampling line; 0139 CO2 Sampling line; 0182 CO2 Sampling lineBarbaras Development, Inc.

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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