Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL

K-Number: K915228 · 1992-02-11

ApplicantHospitak, Inc.
Decision Date1992-02-11
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL is the device name listed in this FDA 510(k) record. The listed applicant is Hospitak, Inc.. It received FDA 510(k) clearance on 1992-02-11 under 510(k) number K915228. 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 DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL?

DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL is a medical device that received FDA 510(k) clearance on 1992-02-11. The listed applicant is Hospitak, Inc.. The 510(k) number is K915228.

When did DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL receive FDA 510(k) clearance?

DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL received FDA 510(k) clearance on 1992-02-11, under 510(k) number K915228.

Who is the listed applicant for DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL?

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

What is the FDA product code for DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL?

The FDA product code for DISPOSABLE CO2 GAS SAMPLING/OXYGEN DELIVERY CANNUL is CCK.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Hospitak, 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.

K955483TRACH MASK MODEL (245, 246)K954787ILLUMINATORK953619WARM N WET HME W/LUER ADAPTERK953620WARM N WET HMEF W/LUER ADAPTERK915750DISPOSABLE BACTERIAL BREATHNG FILTERK920842AEROSOL DELIVERY SYSTEMS

View all 27 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.

↑