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FDA 510(k)

PATIENT GAS SAMPLING LINE FOR OHMEDA 6000

K-Number: K910509 · 1991-04-17

ApplicantIntertech Resources, Inc.
Decision Date1991-04-17
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PATIENT GAS SAMPLING LINE FOR OHMEDA 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1991-04-17 under 510(k) number K910509. 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 PATIENT GAS SAMPLING LINE FOR OHMEDA 6000?

PATIENT GAS SAMPLING LINE FOR OHMEDA 6000 is a medical device that received FDA 510(k) clearance on 1991-04-17. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K910509.

When did PATIENT GAS SAMPLING LINE FOR OHMEDA 6000 receive FDA 510(k) clearance?

PATIENT GAS SAMPLING LINE FOR OHMEDA 6000 received FDA 510(k) clearance on 1991-04-17, under 510(k) number K910509.

Who is the listed applicant for PATIENT GAS SAMPLING LINE FOR OHMEDA 6000?

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

What is the FDA product code for PATIENT GAS SAMPLING LINE FOR OHMEDA 6000?

The FDA product code for PATIENT GAS SAMPLING LINE FOR OHMEDA 6000 is CCK.

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Other records listing Intertech Resources, 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952223XENON GAS BREATHING CIRCUITK952062PFT FILTERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRIC

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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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