meddevicedb.com FDA Device Reference

TELEFLEX ISIS HVT TRACHEAL TUBE, CUFFED, WITH SUBGLOTTIC SECRETION SUCTION PORT

K091761 Class II Abbreviated
Decision Date
2009-10-29
Sponsor / Applicant
Teleflexmedical, Inc.

Technical Specification

510(k) Submission ID K091761
Product Code BTR
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5730
Decision Date 2009-10-29
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TELEFLEX ISIS HVT TRACHEAL TUBE, CUFFED, WITH SUBGLOTTIC SECRETION SUCTION PORT received FDA 510(k) clearance under submission number K091761, sponsored by Teleflexmedical, Inc.. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 2009-10-29.

Classification & Regulation

This clearance is catalogued under FDA product code BTR and 21 CFR 868.5730, within the Anesthesiology review panel as a Class II device.