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FDA 510(k)

TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)

K-Number: K122214 · 2013-05-21

Decision Date2013-05-21
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T) is the device name listed in this FDA 510(k) record. The listed applicant is Nihon Kohden Corp.. It received FDA 510(k) clearance on 2013-05-21 under 510(k) number K122214. 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 TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)?

TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T) is a medical device that received FDA 510(k) clearance on 2013-05-21. The listed applicant is Nihon Kohden Corp.. The 510(k) number is K122214.

When did TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T) receive FDA 510(k) clearance?

TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T) received FDA 510(k) clearance on 2013-05-21, under 510(k) number K122214.

Who is the listed applicant for TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)?

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

What is the FDA product code for TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T)?

The FDA product code for TG-970P SENSOR KIT W/ NEW AIRWAY ADAPTER (YG-213T) 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 Corp. 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 8 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

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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