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FDA 510(k)

GAS SAMPLING NASAL CANNULA

K-Number: K900979 · 1990-03-16

ApplicantGibeck, Inc.
Decision Date1990-03-16
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAS SAMPLING NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Gibeck, Inc.. It received FDA 510(k) clearance on 1990-03-16 under 510(k) number K900979. 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 GAS SAMPLING NASAL CANNULA?

GAS SAMPLING NASAL CANNULA is a medical device that received FDA 510(k) clearance on 1990-03-16. The listed applicant is Gibeck, Inc.. The 510(k) number is K900979.

When did GAS SAMPLING NASAL CANNULA receive FDA 510(k) clearance?

GAS SAMPLING NASAL CANNULA received FDA 510(k) clearance on 1990-03-16, under 510(k) number K900979.

Who is the listed applicant for GAS SAMPLING NASAL CANNULA?

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

What is the FDA product code for GAS SAMPLING NASAL CANNULA?

The FDA product code for GAS SAMPLING NASAL CANNULA is CCK.

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Other records listing Gibeck, Inc. 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.

K965016ISO-GARD FILTER ANGLED(18212)/ISO-GARD FILTER STRAIGHT(19212)K964377THERMAL REGULATION SYSTEM BLANKETK964382HUMID-VENT FILTER COMPACT ANGLED (18402)/HUMID-VENT FILTER COMPACT STRAIGHT(19402)K960511GIBECK WARMBAG REUSABLE CONVECTIVE WARMING BLANKETK954828ISO-GARD HEPA FILTER-HME, ISO-ARD HEPA FILTER-HME W/PORTK953544HUMID-VENT 2 LIGHT/HUMID-VENT 2 PORT LIGHT

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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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