meddevicedb.com FDA Device Reference

Definium Pace Select ET

K242678 Class II Special
Decision Date
2024-10-01
Sponsor / Applicant
Ge Hualun Medical Systems Co. , Ltd.

Technical Specification

510(k) Submission ID K242678
Product Code KPR
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.1680
Decision Date 2024-10-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Definium Pace Select ET received FDA 510(k) clearance under submission number K242678, sponsored by Ge Hualun Medical Systems Co. , Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2024-10-01.

Classification & Regulation

This clearance is catalogued under FDA product code KPR and 21 CFR 892.1680, within the Radiology review panel as a Class II device.