meddevicedb.com FDA Device Reference

SPIROMETER TS-400 SLZ 7547

K855069 Class II Traditional
Decision Date
1986-01-30
Sponsor / Applicant
Teledyne Avionics Div. of Teledyne

Technical Specification

510(k) Submission ID K855069
Product Code BTY
Medical Specialty / Panel Anesthesiology
Regulation Citation 21 CFR 868.1890
Decision Date 1986-01-30
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPIROMETER TS-400 SLZ 7547 received FDA 510(k) clearance under submission number K855069, sponsored by Teledyne Avionics Div. of Teledyne. The device was reviewed via the Traditional premarket notification pathway and assigned to the Anesthesiology review panel. The statutory decision date of record is 1986-01-30.

Classification & Regulation

This clearance is catalogued under FDA product code BTY and 21 CFR 868.1890, within the Anesthesiology review panel as a Class II device.