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FDA 510(k)

DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA

K-Number: K961150 · 1996-09-10

ApplicantHudson Respiratory Care, Inc.
Decision Date1996-09-10
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Respiratory Care, Inc.. It received FDA 510(k) clearance on 1996-09-10 under 510(k) number K961150. 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 DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA?

DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA is a medical device that received FDA 510(k) clearance on 1996-09-10. The listed applicant is Hudson Respiratory Care, Inc.. The 510(k) number is K961150.

When did DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA receive FDA 510(k) clearance?

DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA received FDA 510(k) clearance on 1996-09-10, under 510(k) number K961150.

Who is the listed applicant for DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA?

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

What is the FDA product code for DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA?

The FDA product code for DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA is CCK.

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Other records listing Hudson Respiratory Care, 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.

K031383MODEL 780K011125NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL CANNULA MANUFACTURED BY HRCIK011134OXYGEN SUPPLY TUBING, MODEL 1115K010402SMOOTH-FLO CIRCUITK001213CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40, -50, & -60K993355HUDSON RCI CONCHA COLUMN, CAT. NO. 385-40 AND HUDSON RCI CIRCUIT, CAT. NO. 780-40, 780-41, 780-42, 780-43

View all 15 devices →

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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