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YIELD TISSUE SAMPLER

K090853 Class II Traditional
Decision Date
2009-04-07
Sponsor / Applicant
Broncus Technologies, Inc.

Technical Specification

510(k) Submission ID K090853
Product Code EOQ
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4680
Decision Date 2009-04-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

YIELD TISSUE SAMPLER received FDA 510(k) clearance under submission number K090853, sponsored by Broncus Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 2009-04-07.

Classification & Regulation

This clearance is catalogued under FDA product code EOQ and 21 CFR 874.4680, within the Ear, Nose, Throat review panel as a Class II device.