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FDA 510(k)

RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY

K-Number: K961840 · 1996-06-27

ApplicantRusch Intl.
Decision Date1996-06-27
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY is the device name listed in this FDA 510(k) record. The listed applicant is Rusch Intl.. It received FDA 510(k) clearance on 1996-06-27 under 510(k) number K961840. 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 RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY?

RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY is a medical device that received FDA 510(k) clearance on 1996-06-27. The listed applicant is Rusch Intl.. The 510(k) number is K961840.

When did RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY receive FDA 510(k) clearance?

RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY received FDA 510(k) clearance on 1996-06-27, under 510(k) number K961840.

Who is the listed applicant for RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY?

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

What is the FDA product code for RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY?

The FDA product code for RUSCH ORAL/NASAL TRACHEAL TUBE, PLAIN MAGILL/MURPHY is BTR.

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Other records listing Rusch Intl. 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.

K033023INTERMITTENT URETHRAL CATHETERSK030559RUSCH POLYFLEX STENT FOR THE ESOPHAGUS W/INTRODUCER/DELIVERY SYSTEMK023666RUSCH GUIDED CHOLANGIOGRAPHY CATHETERK023918RUSCH CRYSTAL CLEAR TRACHEOSTOMY SETS, CUFFED AND CUFFLESSK023964RUSCH MICROLARYNGEAL TUBEK021540RUSCH EDGAR TUBE

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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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