Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES

K-Number: K873742 · 1987-10-01

ApplicantHood Laboratories
Decision Date1987-10-01
Product CodeNWA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES is the device name listed in this FDA 510(k) record. The listed applicant is Hood Laboratories. It received FDA 510(k) clearance on 1987-10-01 under 510(k) number K873742. 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 HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES?

HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES is a medical device that received FDA 510(k) clearance on 1987-10-01. The listed applicant is Hood Laboratories. The 510(k) number is K873742.

When did HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES receive FDA 510(k) clearance?

HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES received FDA 510(k) clearance on 1987-10-01, under 510(k) number K873742.

Who is the listed applicant for HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES?

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

What is the FDA product code for HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES?

The FDA product code for HOOD TRACHEAL & TRACHEAL-BRONCHIAL PROSTHESES 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 Hood Laboratories 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.

K921452ACOUSTIC RHINOMETERK920994HOOD NASAL SEPTAL BUTTONK905703KRUPIN EYE VALVE WITH DISKK904821ELIACHAR MODIFIED ESOPHAGEAL STENTK897049GIBSON ENDOLYMPHATIC SHUNTK897059HOOD SPEAKING VALVE

View all 19 devices →

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 SAK894380DUMON TRACHEOBRONCHIAL STENTBryan Corp.

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.

↑