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FDA 510(k)

MODIFIED GAS SAMPLING KIT

K-Number: K863640 · 1986-10-08

ApplicantRespiratory Support Products, Inc.
Decision Date1986-10-08
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED GAS SAMPLING KIT is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1986-10-08 under 510(k) number K863640. 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 MODIFIED GAS SAMPLING KIT?

MODIFIED GAS SAMPLING KIT is a medical device that received FDA 510(k) clearance on 1986-10-08. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K863640.

When did MODIFIED GAS SAMPLING KIT receive FDA 510(k) clearance?

MODIFIED GAS SAMPLING KIT received FDA 510(k) clearance on 1986-10-08, under 510(k) number K863640.

Who is the listed applicant for MODIFIED GAS SAMPLING KIT?

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

What is the FDA product code for MODIFIED GAS SAMPLING KIT?

The FDA product code for MODIFIED GAS SAMPLING KIT is CCK.

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Other records listing Respiratory Support Products, 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.

K983862CLOUD 1 HUMIDIFICATION SYSTEMK921190ADAP-TEMP TEMPERATURE SENSOR ADAPTERK920469MYOCARDINAL TEMPERATURE SENSOR WITH TYPE 400 SERIEK921510GAS SAMPLING KIT MODIFICATIONK913082BI-TEMP TEMPERATURE MONITOR,MODEL TM-300DK912280BI-TEMP TEMPERATURE MONITOR, MODEL TM-400D

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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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