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BASAL DIGITAL THERMOMETER

K141505 Class II Special
Decision Date
2014-08-26
Sponsor / Applicant
K-Jump Health Co., Ltd.

Technical Specification

510(k) Submission ID K141505
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 2014-08-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BASAL DIGITAL THERMOMETER received FDA 510(k) clearance under submission number K141505, sponsored by K-Jump Health Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2014-08-26.

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.