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FDA 510(k)

YG-125T AND YG-135T NASAL ADAPTER

K-Number: K072843 · 2007-11-29

Decision Date2007-11-29
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

YG-125T AND YG-135T NASAL ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden America, Inc.. It received FDA 510(k) clearance on 2007-11-29 under 510(k) number K072843. 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 YG-125T AND YG-135T NASAL ADAPTER?

YG-125T AND YG-135T NASAL ADAPTER is a medical device that received FDA 510(k) clearance on 2007-11-29. The listed applicant is Nihon Kohden America, Inc.. The 510(k) number is K072843.

When did YG-125T AND YG-135T NASAL ADAPTER receive FDA 510(k) clearance?

YG-125T AND YG-135T NASAL ADAPTER received FDA 510(k) clearance on 2007-11-29, under 510(k) number K072843.

Who is the listed applicant for YG-125T AND YG-135T NASAL ADAPTER?

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

What is the FDA product code for YG-125T AND YG-135T NASAL ADAPTER?

The FDA product code for YG-125T AND YG-135T NASAL ADAPTER 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.

Other records listing Nihon Kohden America, 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.

View all 166 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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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