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FDA 510(k)

DUMON TRACHEOBRONCHIAL STENT

K-Number: K894380 · 1989-10-24

ApplicantBryan Corp.
Decision Date1989-10-24
Product CodeNWA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DUMON TRACHEOBRONCHIAL STENT is the device name listed in this FDA 510(k) record. The listed applicant is Bryan Corp.. It received FDA 510(k) clearance on 1989-10-24 under 510(k) number K894380. The device is classified under product code NWA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUMON TRACHEOBRONCHIAL STENT?

DUMON TRACHEOBRONCHIAL STENT is a medical device that received FDA 510(k) clearance on 1989-10-24. The listed applicant is Bryan Corp.. The 510(k) number is K894380.

When did DUMON TRACHEOBRONCHIAL STENT receive FDA 510(k) clearance?

DUMON TRACHEOBRONCHIAL STENT received FDA 510(k) clearance on 1989-10-24, under 510(k) number K894380.

Who is the listed applicant for DUMON TRACHEOBRONCHIAL STENT?

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

What is the FDA product code for DUMON TRACHEOBRONCHIAL STENT?

The FDA product code for DUMON TRACHEOBRONCHIAL STENT is NWA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Bryan Corp. 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.

K002063BIOTRACE, MODEL 1730K913242MICROPROCESSED CONTROLLED LAPAROFLATORK881249BAGGISH, HYSTEROSCOPEK854414DUMON/HARRELL

Related Devices (Code: NWA)

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.

K261541VisionAir Enhanced Stock StentVisionAir SolutionsK243126TRACHEOBRONXANE™ DUMON®Novatech SAK213969VisionAir Patient-Specific Airway StentNew Cos Inc. Dba Visionair SolutionsK182743Patient-Specific Airway StentNew Cos, Inc.K971509ENDOXANENovatech SAK873742HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESESHood Laboratories

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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