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FDA 510(k)

END TIDAL CO2 OPTION B

K-Number: K930524 · 1994-02-07

ApplicantMedical Data Electronics
Decision Date1994-02-07
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

END TIDAL CO2 OPTION B is the device name listed in this FDA 510(k) record. The listed applicant is Medical Data Electronics. It received FDA 510(k) clearance on 1994-02-07 under 510(k) number K930524. 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 END TIDAL CO2 OPTION B?

END TIDAL CO2 OPTION B is a medical device that received FDA 510(k) clearance on 1994-02-07. The listed applicant is Medical Data Electronics. The 510(k) number is K930524.

When did END TIDAL CO2 OPTION B receive FDA 510(k) clearance?

END TIDAL CO2 OPTION B received FDA 510(k) clearance on 1994-02-07, under 510(k) number K930524.

Who is the listed applicant for END TIDAL CO2 OPTION B?

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

What is the FDA product code for END TIDAL CO2 OPTION B?

The FDA product code for END TIDAL CO2 OPTION B is CCK.

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Other records listing Medical Data Electronics 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.

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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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