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FDA 510(k)

SERIES 7000 END TIDAL CO2 MONITORING SYSTEM

K-Number: K851001 · 1985-05-13

ApplicantMarquette Electronics, Inc.
Decision Date1985-05-13
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERIES 7000 END TIDAL CO2 MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Marquette Electronics, Inc.. It received FDA 510(k) clearance on 1985-05-13 under 510(k) number K851001. 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 SERIES 7000 END TIDAL CO2 MONITORING SYSTEM?

SERIES 7000 END TIDAL CO2 MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-05-13. The listed applicant is Marquette Electronics, Inc.. The 510(k) number is K851001.

When did SERIES 7000 END TIDAL CO2 MONITORING SYSTEM receive FDA 510(k) clearance?

SERIES 7000 END TIDAL CO2 MONITORING SYSTEM received FDA 510(k) clearance on 1985-05-13, under 510(k) number K851001.

Who is the listed applicant for SERIES 7000 END TIDAL CO2 MONITORING SYSTEM?

The FDA 510(k) record lists Marquette Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERIES 7000 END TIDAL CO2 MONITORING SYSTEM?

The FDA product code for SERIES 7000 END TIDAL CO2 MONITORING SYSTEM is CCK.

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Other records listing Marquette Electronics, Inc. as applicant

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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.

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

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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