meddevicedb.com FDA Device Reference

CLEANING KIT CARE & CLEANING OF TRACHEAL T-TUBE

K853419 Class II Traditional
Decision Date
1985-12-06
Sponsor / Applicant
Hood Laboratories

Technical Specification

510(k) Submission ID K853419
Product Code BTO
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.5800
Decision Date 1985-12-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CLEANING KIT CARE & CLEANING OF TRACHEAL T-TUBE received FDA 510(k) clearance under submission number K853419, sponsored by Hood Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1985-12-06.

Classification & Regulation

This clearance is catalogued under FDA product code BTO and 21 CFR 868.5800, within the Anesthesiology review panel as a Class II device.