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FIVE STAR BRONCHOSCOPE

K960876 Class II Traditional
Decision Date
1996-05-08
Sponsor / Applicant
Five Star Medical, Inc.

Technical Specification

510(k) Submission ID K960876
Product Code EOB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4760
Decision Date 1996-05-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIVE STAR BRONCHOSCOPE received FDA 510(k) clearance under submission number K960876, sponsored by Five Star Medical, 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 1996-05-08.

Classification & Regulation

This clearance is catalogued under FDA product code EOB and 21 CFR 874.4760, within the Ear, Nose, Throat review panel as a Class II device.