meddevicedb.com FDA Device Reference

WIRELESS THERMOMETER

K132761 Class II Traditional
Decision Date
2014-07-08
Sponsor / Applicant
Raiing Medical Company

Technical Specification

510(k) Submission ID K132761
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2014-07-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WIRELESS THERMOMETER received FDA 510(k) clearance under submission number K132761, sponsored by Raiing Medical Company. 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 2014-07-08.

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.