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FLUOROPLASTIC VENTILATION TUBES

K992222 Class II Traditional
Decision Date
1999-08-26
Sponsor / Applicant
Gyrus Ent LLC

Technical Specification

510(k) Submission ID K992222
Product Code ETD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3880
Decision Date 1999-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUOROPLASTIC VENTILATION TUBES received FDA 510(k) clearance under submission number K992222, sponsored by Gyrus Ent LLC. 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 1999-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code ETD and 21 CFR 874.3880, within the Ear, Nose, Throat review panel as a Class II device.