meddevicedb.com FDA Device Reference

ELECTRONIC THERMOMETER

K780800 Class II Traditional
Decision Date
1978-06-06
Sponsor / Applicant
Metek Corp.

Technical Specification

510(k) Submission ID K780800
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1978-06-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRONIC THERMOMETER received FDA 510(k) clearance under submission number K780800, sponsored by Metek Corp.. 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 1978-06-06.

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.