meddevicedb.com FDA Device Reference

ELECTRONIC DIGITAL THERMOMETER

K883005 Class II Traditional
Decision Date
1988-08-04
Sponsor / Applicant
Hanson Scale Co.

Technical Specification

510(k) Submission ID K883005
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1988-08-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECTRONIC DIGITAL THERMOMETER received FDA 510(k) clearance under submission number K883005, sponsored by Hanson Scale Co.. 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 1988-08-04.

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.