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

FDA 510(k)

BroncTru™ Transbronchial Access Tool

K-Number: K232601 · 2024-05-31

Decision Date2024-05-31
Product CodeEOQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BroncTru™ Transbronchial Access Tool is a medical device manufactured by Broncus Medical, Inc.. It received FDA 510(k) clearance on 2024-05-31 under approval number K232601. The device is classified under product code EOQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BroncTru™ Transbronchial Access Tool?

BroncTru™ Transbronchial Access Tool is a medical device that received FDA 510(k) clearance on 2024-05-31. It is manufactured by Broncus Medical, Inc.. The 510(k) number is K232601.

When was BroncTru™ Transbronchial Access Tool approved by the FDA?

BroncTru™ Transbronchial Access Tool received FDA 510(k) clearance on 2024-05-31, under approval number K232601.

What company makes BroncTru™ Transbronchial Access Tool?

BroncTru™ Transbronchial Access Tool is manufactured by Broncus Medical, Inc..

What is the FDA product code for BroncTru™ Transbronchial Access Tool?

The FDA product code for BroncTru™ Transbronchial Access Tool is EOQ.

Related Clinical Trials

Other Devices by Broncus Medical, Inc.

Related Devices (Code: EOQ)

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.