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FDA 510(k)

OHIO DISPOSABLE TRACHEAL TUBE

K-Number: K810763 · 1981-03-27

ApplicantAirco/Ohio Medical Products
Decision Date1981-03-27
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 Airco/Ohio Medical Products. It received FDA 510(k) clearance on 1981-03-27 under 510(k) number K810763. 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 1981-03-27. The listed applicant is Airco/Ohio Medical Products. The 510(k) number is K810763.

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

OHIO DISPOSABLE TRACHEAL TUBE received FDA 510(k) clearance on 1981-03-27, under 510(k) number K810763.

Who is the listed applicant for OHIO DISPOSABLE TRACHEAL TUBE?

The FDA 510(k) record lists Airco/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.

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Other records listing Airco/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.

K833459COAXIAL VOL. VENTILATOR CIRCUITK833452OHIO GMS ABSORBERK832418OHIO TEMPERATURE SIMULATORK832565OHIO 5400 VOLUME MONITORK832185OHIO MODEL 922 SPIROMETERK830446OXYGEN MONITOR OHIO 5100

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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.

K251794Tenax® Laser Resistant Endotracheal TubeBryan Medical, Inc.K253437Spiro-VISTASpiro RoboticsK250173Shiley™ Oral RAE Tracheal Tube Cuffless, Murphy Eye (113-XX) Shiley™ Nasal RAE Tracheal Tube Cuffless, Murphy Eye (114-XX) Shiley™ Oral RAE Tracheal Tube Cuffed, Murphy Eye (115-XX) Shiley™ Oral RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (115-XXOR) Shiley™ Nasal RAE Tracheal Tube with TaperGuard™ Cuff, Murphy Eye (119-XXNR)Covidien, LLCK243785Shiley™ Oral/Nasal Tracheal Tube with TaperGuard™ Cuff Reinforced, Murphy Eye Shiley™ Tracheal Tube TaperGuard™ Cuff Reinforced with Stylet Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced Shiley™ Lo-Contour Oral/Nasal Tracheal Tube Cuffed Reinforced, Murphy Eye Shiley™ Oral/Nasal Tracheal Tube Cuffless ReinforcedCovidien, LLCK243579AeroJet Ventilation CatheterPipeline Medical Products, LLCK251499Frova Intubating Introducer (C-CAE-14.0-70-FII); Frova Intubating Introducer (C-CAE-14.0-70-FI); Frova Intubating Introducer (C-CAE-14.0-70-FIC); Frova Intubating Introducer (C-CAE-14.0-70-FIC-SPOPS)William Cook Europe Aps

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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