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RUSCH PEDIATRIC REINFORCED TRAHEAL (OR ENDOTRACHEAL) TUBE - UNCUFFED, STERILE

K954585 Class II Traditional
Decision Date
1996-05-10
Sponsor / Applicant
Rusch Intl.

Technical Specification

510(k) Submission ID K954585
Product Code BTR
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5730
Decision Date 1996-05-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RUSCH PEDIATRIC REINFORCED TRAHEAL (OR ENDOTRACHEAL) TUBE - UNCUFFED, STERILE received FDA 510(k) clearance under submission number K954585, sponsored by Rusch Intl.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1996-05-10.

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.