meddevicedb.com FDA Device Reference

HI-LO TEMP TYMPANIC TEMP. SENSOR

K832635 Class II Traditional
Decision Date
1983-10-04
Sponsor / Applicant
Mallinckrodt Critical Care

Technical Specification

510(k) Submission ID K832635
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1983-10-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HI-LO TEMP TYMPANIC TEMP. SENSOR received FDA 510(k) clearance under submission number K832635, sponsored by Mallinckrodt Critical Care. 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 1983-10-04.

Classification & Regulation

This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.