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FDA 510(k)

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000

K-Number: K982943 · 1999-07-12

Decision Date1999-07-12
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000 is the device name listed in this FDA 510(k) record. The listed applicant is Transtracheal Systems. It received FDA 510(k) clearance on 1999-07-12 under 510(k) number K982943. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000?

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000 is a medical device that received FDA 510(k) clearance on 1999-07-12. The listed applicant is Transtracheal Systems. The 510(k) number is K982943.

When did TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000 receive FDA 510(k) clearance?

TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000 received FDA 510(k) clearance on 1999-07-12, under 510(k) number K982943.

Who is the listed applicant for TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000?

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

What is the FDA product code for TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000?

The FDA product code for TRANSTRACHEAL DEMAND OXYGEN CONTROLLER MODEL DOC-3000 is NFB.

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 Transtracheal Systems 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: NFB)

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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