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FDA 510(k)

MASSTRON/MARQUEST MT-1000 GAS ANALYZER

K-Number: K871253 · 1987-06-15

ApplicantMasstron C/O Burditt, Bowles & Radzius, Ltd.
Decision Date1987-06-15
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MASSTRON/MARQUEST MT-1000 GAS ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Masstron C/O Burditt, Bowles & Radzius, Ltd.. It received FDA 510(k) clearance on 1987-06-15 under 510(k) number K871253. 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 MASSTRON/MARQUEST MT-1000 GAS ANALYZER?

MASSTRON/MARQUEST MT-1000 GAS ANALYZER is a medical device that received FDA 510(k) clearance on 1987-06-15. The listed applicant is Masstron C/O Burditt, Bowles & Radzius, Ltd.. The 510(k) number is K871253.

When did MASSTRON/MARQUEST MT-1000 GAS ANALYZER receive FDA 510(k) clearance?

MASSTRON/MARQUEST MT-1000 GAS ANALYZER received FDA 510(k) clearance on 1987-06-15, under 510(k) number K871253.

Who is the listed applicant for MASSTRON/MARQUEST MT-1000 GAS ANALYZER?

The FDA 510(k) record lists Masstron C/O Burditt, Bowles & Radzius, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASSTRON/MARQUEST MT-1000 GAS ANALYZER?

The FDA product code for MASSTRON/MARQUEST MT-1000 GAS ANALYZER is CCK.

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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.

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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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