meddevicedb.com FDA Device Reference

THERMOSCAN-INSTANT THERMOMETER MODEL IR-4000

K902912 Class II Traditional
Decision Date
1990-07-24
Sponsor / Applicant
Thermoscan, Inc.

Technical Specification

510(k) Submission ID K902912
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1990-07-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

THERMOSCAN-INSTANT THERMOMETER MODEL IR-4000 received FDA 510(k) clearance under submission number K902912, sponsored by Thermoscan, 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 1990-07-24.

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.