meddevicedb.com FDA Device Reference

PACI-TEMP, PACIFIER WITH DIGITAL THERMOMETER

K952073 Class II Traditional
Decision Date
1995-12-18
Sponsor / Applicant
Intelligent Product Limited Co.

Technical Specification

510(k) Submission ID K952073
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1995-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PACI-TEMP, PACIFIER WITH DIGITAL THERMOMETER received FDA 510(k) clearance under submission number K952073, sponsored by Intelligent Product Limited 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 1995-12-18.

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.