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FDA 510(k)

OHIO DISPOSABLE TRACHEAL TUBE

K-Number: K800634 · 1980-04-02

Decision Date1980-04-02
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OHIO DISPOSABLE TRACHEAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Ohio Medical Products. It received FDA 510(k) clearance on 1980-04-02 under 510(k) number K800634. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OHIO DISPOSABLE TRACHEAL TUBE?

OHIO DISPOSABLE TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1980-04-02. The listed applicant is Ohio Medical Products. The 510(k) number is K800634.

When did OHIO DISPOSABLE TRACHEAL TUBE receive FDA 510(k) clearance?

OHIO DISPOSABLE TRACHEAL TUBE received FDA 510(k) clearance on 1980-04-02, under 510(k) number K800634.

Who is the listed applicant for OHIO DISPOSABLE TRACHEAL TUBE?

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

What is the FDA product code for OHIO DISPOSABLE TRACHEAL TUBE?

The FDA product code for OHIO DISPOSABLE TRACHEAL TUBE is BTR.

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 Ohio Medical Products 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 47 devices →

Related Devices (Code: BTR)

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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