meddevicedb.com FDA Device Reference

Disposable Temperature Probe

K181967 Class II Traditional
Decision Date
2018-12-10
Sponsor / Applicant
Shenzhen Launch Electrical Co., Ltd.

Technical Specification

510(k) Submission ID K181967
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2018-12-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Disposable Temperature Probe received FDA 510(k) clearance under submission number K181967, sponsored by Shenzhen Launch Electrical Co., Ltd.. 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 2018-12-10.

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.