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FDA 510(k)

WIRE REINFORCED ENDOTRACHEAL TUBE

K-Number: K932647 · 1993-11-02

ApplicantVitaid, Ltd.
Decision Date1993-11-02
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

WIRE REINFORCED ENDOTRACHEAL TUBE is the device name listed in this FDA 510(k) record. The listed applicant is Vitaid, Ltd.. It received FDA 510(k) clearance on 1993-11-02 under 510(k) number K932647. 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 WIRE REINFORCED ENDOTRACHEAL TUBE?

WIRE REINFORCED ENDOTRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1993-11-02. The listed applicant is Vitaid, Ltd.. The 510(k) number is K932647.

When did WIRE REINFORCED ENDOTRACHEAL TUBE receive FDA 510(k) clearance?

WIRE REINFORCED ENDOTRACHEAL TUBE received FDA 510(k) clearance on 1993-11-02, under 510(k) number K932647.

Who is the listed applicant for WIRE REINFORCED ENDOTRACHEAL TUBE?

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

What is the FDA product code for WIRE REINFORCED ENDOTRACHEAL TUBE?

The FDA product code for WIRE REINFORCED ENDOTRACHEAL TUBE is BTR.

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Other records listing Vitaid, Ltd. 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.

K050803PEDIATRIC CUFFED AND UNCUFFED ET TUBES; STANDARD CUFFED AND UNCUFFED ET TUBESK901738SELFCATHK894883PHYCON ALL SILICONE BALLOON CATHETERK894794AGISHI ASCITES PUMP PERITONEOCAVAL SHUNT PUMPK894669LASER SHIELDING TUBEK894337UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM

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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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