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FDA 510(k)

INFINITY MCABLE - MAINSTREAM CO2

K-Number: K100941 · 2010-04-23

ApplicantDraeger Medical AG & Co. KG
Decision Date2010-04-23
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INFINITY MCABLE - MAINSTREAM CO2 is the device name listed in this FDA 510(k) record. The listed applicant is Draeger Medical AG & Co. KG. It received FDA 510(k) clearance on 2010-04-23 under 510(k) number K100941. 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 INFINITY MCABLE - MAINSTREAM CO2?

INFINITY MCABLE - MAINSTREAM CO2 is a medical device that received FDA 510(k) clearance on 2010-04-23. The listed applicant is Draeger Medical AG & Co. KG. The 510(k) number is K100941.

When did INFINITY MCABLE - MAINSTREAM CO2 receive FDA 510(k) clearance?

INFINITY MCABLE - MAINSTREAM CO2 received FDA 510(k) clearance on 2010-04-23, under 510(k) number K100941.

Who is the listed applicant for INFINITY MCABLE - MAINSTREAM CO2?

The FDA 510(k) record lists Draeger Medical AG & Co. KG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFINITY MCABLE - MAINSTREAM CO2?

The FDA product code for INFINITY MCABLE - MAINSTREAM CO2 is CCK.

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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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