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FDA 510(k)

IL MODEL END TIDAL CO2 ANALYZER

K-Number: K791570 · 1979-09-04

ApplicantInstrumentation Laboratory CO
Decision Date1979-09-04
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IL MODEL END TIDAL CO2 ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Instrumentation Laboratory CO. It received FDA 510(k) clearance on 1979-09-04 under 510(k) number K791570. 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 IL MODEL END TIDAL CO2 ANALYZER?

IL MODEL END TIDAL CO2 ANALYZER is a medical device that received FDA 510(k) clearance on 1979-09-04. The listed applicant is Instrumentation Laboratory CO. The 510(k) number is K791570.

When did IL MODEL END TIDAL CO2 ANALYZER receive FDA 510(k) clearance?

IL MODEL END TIDAL CO2 ANALYZER received FDA 510(k) clearance on 1979-09-04, under 510(k) number K791570.

Who is the listed applicant for IL MODEL END TIDAL CO2 ANALYZER?

The FDA 510(k) record lists Instrumentation Laboratory CO as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IL MODEL END TIDAL CO2 ANALYZER?

The FDA product code for IL MODEL END TIDAL CO2 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.

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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