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FDA 510(k)

DISPOSABLE GAS SAMPLING LINES

K-Number: K946044 · 1994-12-27

ApplicantCatheter Research, Inc.
Decision Date1994-12-27
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE GAS SAMPLING LINES is the device name listed in this FDA 510(k) record. The listed applicant is Catheter Research, Inc.. It received FDA 510(k) clearance on 1994-12-27 under 510(k) number K946044. 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 GAS SAMPLING LINES?

DISPOSABLE GAS SAMPLING LINES is a medical device that received FDA 510(k) clearance on 1994-12-27. The listed applicant is Catheter Research, Inc.. The 510(k) number is K946044.

When did DISPOSABLE GAS SAMPLING LINES receive FDA 510(k) clearance?

DISPOSABLE GAS SAMPLING LINES received FDA 510(k) clearance on 1994-12-27, under 510(k) number K946044.

Who is the listed applicant for DISPOSABLE GAS SAMPLING LINES?

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

What is the FDA product code for DISPOSABLE GAS SAMPLING LINES?

The FDA product code for DISPOSABLE GAS SAMPLING LINES is CCK.

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Other records listing Catheter Research, 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.

K123258THE ADVANCE CATHETER FOR HSG AND SISK120154INTRAUTERINE INSEMINATION (IUI) CATHETERK032835H/S CATHETER SETK020292UTERINE INJECTORK973839DISPOSABLE ESOPHAGEAL STETHOSCOPEK974357UTERINE MANIPULATOR/INJECTOR

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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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