meddevicedb.com FDA Device Reference

TEMPO2-I DISPOSABLE THERMOMETERS

K790890 Class I Traditional
Decision Date
1979-06-27
Sponsor / Applicant
Airlife, Inc.

Technical Specification

510(k) Submission ID K790890
Product Code FQZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2900
Decision Date 1979-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TEMPO2-I DISPOSABLE THERMOMETERS received FDA 510(k) clearance under submission number K790890, sponsored by Airlife, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1979-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code FQZ and 21 CFR 880.2900, within the General Hospital review panel as a Class I device.